Associate Research Scientist - Advanced Preformulation,

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					FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Research Scientist/Sr. Research Scientist, Analytical Method Development Research & Development Commack, NY Description of Duties and Responsibilities:  Developing and validate routine testing methods to the R&D Analytical Pharmaceutical Laboratory  Ensure procedures conforms to appropriate standards of identity, strength, quality and purity for components, bulk and finished products, scale-up samples, process validation samples, cleaning validation samples, marketed stability samples, affiliate samples and international manufacturing samples  Ensure training programs are properly developed and implemented  Ensure that the Laboratory Analysts are technically developed  Coordinate the laboratory equipment qualifications, calibrations and preventative maintenance programs as needed  Coordinate internal laboratory projects  Develop and implement systems and training to ensure successful completion of these projects  Audit/Review all laboratory data for approval to next step  Develop and implement local laboratory policies and procedures  Audit the laboratory for compliance to cGMPs and safety requirements  Develop procedures, systems, practices to ensure compliance to all regulatory requirements  Recommend the need for new equipment to serve expanding operational and regulatory requirements sufficiently in advance of the need  Ensure specific objectives and goals of the department are met  Candidate will work independently Requirements:  PhD with 0-8 years in methods development in relevant pharmaceutical development area. Must have strong chromatography exp. Preference given to candidates with pharmaceutical industry experience.  Strong HPLC, computer, written and oral communications and troubleshooting skills are required. LC/MS experience is desirable. GC, MS, IR, thermal techniques a plus. To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Research Scientist, Synthesis Analytical Research and Development Commack, NY Description of Duties and Responsibilities: Process Chemical route discovery and development  Demonstrate safe, scaleable and economical synthesis of APIs up to kilo-lab scale  Optimize existing processes.  Supply materials from mg to kg.

Requirements:  PhD in Organic Chemistry with 5+ years relevant pharmaceutical industry experience and a track record of innovation.  Experience in technology transfer to CMOs and working with third party drug manufacturers.  Medicinal Chemistry experience is a plus. To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 E-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Project Leader, Analytical Services Analytical Research and Development Commack, NY Description of Duties and Responsibilities:  Experience with HPLC/GC, UV spec, dissolution, stability testing; HPLC; UV Spec  Should be able to troubleshoot methods and instruments and have good knowledge of data acquisition systems.  Candidate should demonstrate some level of supervisory skills as well as motivate and teach the person working under them.  Candidate should be independent, a self-starter, and be able to work as a team.

Requirements:  BS with 5-7 years exp or MS with 3-5 years in Pharmaceutical R&D,  Should have working knowledge of cGLP/cGMPs and knowledge of correcting or rejecting data based on scientific rationale, understand all chemistry and pharmaceutical analysis To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Scientist II/III, Drug Characterization Analytical Research and Development Commack, NY Position Summary: The analysis, disposition and release of Excipients, Active Drug Substances (API) and Reference Standards. Description of Duties and Responsibilities:  Analyze bulk pharmaceutical samples.  Analyze excipient samples.  Conduct analyses according to written protocols for the performance of material characterization studies.  Analyze finished pharmaceutical samples.  Carry out investigations when necessary.  Identify and provide resolution for complex problems related to methodologies, sample analyses and laboratory systems.  Provide leadership and supervision for maintenance tasks of the laboratory instruments.  Provide training to junior level chemists on basic operating procedures.  Act a project manager for various laboratory studies.  Communicate in a professional manner with representatives of contract laboratories. Requirements:  B.S. with 3-5 years or M.S. with 2-4 years of Analytical experience in pharmaceutical field.  Candidate must have first hand experience in analytical instruments that include HPLC, GC, FTIR, DSC, TGA and XRD.  Candidate should have a broad knowledge of good manufacturing practices (GMP).  Candidate should have the ability to work in a project team environment, have excellent oral and written communication skills. To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Manager/Associate Director, CMC Analytical Research & Development Commack, NY Description of Duties and Responsibilities: Manage all CMC activities with the Forest Laboratories R & D organization to support drug development programs  Direct the activities of a group of 4 to 6 scientists and technical staff who are responsible for the preparation of chemistry, manufacturing and control (CMC) documents for FDA submissions  Prepare, coordinate and manage the process of assembling and submitting the CMC portion of Forest’s regulatory documents. This includes documents and information required for IND and NDA submissions  Serve as the principle representative of Forest Laboratories in interactions with the Drug Regulatory Affairs group and with the FDA on all CMC matters relating to pharmaceutical development projects  Develop and maintain a strong working knowledge of CDER guidelines and the application of these guidelines to the CMC portion of regulatory submissions  Provide leadership in the migration to the CTD format and e-Submission  Coordinate activities and provide guidance for internal functional groups to ensure acceptance and fileability of documents  Interact with scientists and technical staff in the Analytical Chemistry and Formulations Development Departments in an informative and collaborative fashion which supports pharmaceutical development  Provide oral and written reports as necessary to R & D management on matters relating to CMC activities  Provide benefit/risk assessments to senior management Requirements:  Ph.D. in Analytical Chemistry or a related discipline with 4-8 years of relevant experience  Strong working knowledge of CMC activities including CDER guidelines  Excellent oral and written communication skills  Orientation to detail and a recognition of the importance of accurately interpreting and applying regulatory guidelines To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Director/Senior Director, CMC Analytical Research & Development Commack, NY Description of Duties and Responsibilities:  Manager stability group and routine stability reporting  Manage all CMC activities with the Forest Laboratories R & D organization to support drug development programs  Direct the activities of a CMC group (scientists and technical staff) who are responsible for the preparation of chemistry, manufacturing and control (CMC) documents for FDA submissions  Prepare, coordinate and manage the process of assembling and submitting the CMC portion of Forest’s regulatory documents. This includes documents and information required for IND and NDA submissions  Serve as the principle representative of Forest Laboratories in interactions with the Drug Regulatory Affairs group and with the FDA on all CMC matters relating to pharmaceutical development projects  Develop and maintain a strong working knowledge of CDER guidelines and the application of these guidelines to the CMC portion of regulatory submissions  Provide leadership in the migration to the CTD format and e-Submission  Coordinate activities and provide guidance for internal functional groups to ensure acceptance and fileability of documents  Interact with scientists and technical staff in the Analytical Chemistry and Formulations Development Departments in an informative and collaborative fashion which supports pharmaceutical development  Provide oral and written reports as necessary to R & D management on matters relating to CMC activities  Provide benefit/risk assessments to senior management Requirements:  Ph.D. in Analytical Chemistry or a related discipline with 10+ years of relevant experience  Strong working knowledge of CMC activities including CDER guidelines  Excellent oral and written communication skills  Orientation to detail and a recognition of the importance of accurately interpreting and applying regulatory guidelines To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Technical Writer, CMC Analytical Research & Development Commack, NY Requirements:  2 positions: BS/MS with 2-4 years exp and BS/MS with 6-10 yrs exp or Ph.D. with 2-4 yrs exp in the pharmaceutical research field.  Demonstrate experience in the pharmaceutical industry having either worked in related areas in pharmaceutical R&D (analytical, formulation/preformulation, process/ chemical development, etc.), Quality Assurance or Regulatory Affairs  Familiarity with (FDA) regulatory guidelines and cGMP/cGLP guidances are essential  Prior experience in the preparation of patents, technical publications, and regulatory dossiers including DMF’s, CMC sections of IND’s/ NDA’s and MAA’s is highly desirable  Prior exp to CTD and/or electronic submission is a plus  Must demonstrate good oral and written communication skills  Should positively demonstrate ability to work in a team environment. Preference will be given to candidates with exp and working knowledge in pharmaceutical development program and project team leadership skills  Candidate must have experience with Documentum (electronic submissions) To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Documentum Specialist, CMC Analytical Research & Development Commack, NY Requirements:  BS/MS with 6-10 yrs exp in the pharmaceutical research field.

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Previous experience with developing, maintaining, and controlling electronic filing and hard copy systems for all types of pharmaceutical R&D documentation generated in support of IND, NDA, and ANDA submissions (ie. SOP's, specifications, analytical methods, protocols, development reports, analytical test results, batch records, training records, validations, change control, technical publications, etc.) High level knowledge of Documentum functions and capabilities required.



To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Associate Director/Director, Bioanalytical and Drug Metabolism Projects Research and Development Farmingdale, NY Description of Duties and Responsibilities:  Candidate will be supervising lead scientists to conduct all phases of bioassays to support pharmacokinetics, toxicokinetics and ADME studies.  Candidate will accept study results, review study reports, prepare position paper and submission documents, and interacting with QA group.  Candidate will also participate in reviewing method development and validation, protocol design, evaluation of literature data, study documents from research partners and contract research organization.  Candidate will assist Department Head in resource, time line and budget planning. Candidate will supervise senior level scientists and assist them in their career development.  This senior position is also responsible for preparing or reviewing relevant bioanalytical methods, data and summaries for submission (IND and NDA).  This position is also responsible for summarizing metabolism data from internal or external sources. Qualifications:  Ph.D. degree in Bioanalytical Chemistry, Pharmaceutical Science or related field with minimum 12+ years of bioanalytical/ADME studies leadership experience in US pharmaceutical R&D with at least 7+ years of supervisory experience with Ph.D. level staff.  Experience in product development phase activities with some late discovery phase support is desired.  Candidate must have a good perspective of ADME issues in drug development and regulatory submission.  Will consider CRO experience with strong project management, compliance, communication and people skills.  Candidate must have hands on experience in bioanalysis that include instrumentation (HPLC, LC/MS/MS and liquid scintillation counting techniques), chromatography, solution chemistry, extraction techniques (e.g. SPE), automation (liquid handler, 96-well format), and electronic LIMS (WATSON). Candidate should have direct working experience in GLP and regulatory submission . To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Research Scientist, Bioanalytical and Drug Metabolism Research and Development Farmingdale, NY Description of Duties and Responsibilities:  Develop bioanalytical methods to support pharmacokinetics, toxicokinetics and ADME studies.  Candidate will also assist in reviewing study protocols, evaluation of literature data, review study documents from research partners and contract research organization.  Candidate will accept method validation and stability results, responsible for preparing method reports, position paper and submission documents, and interacting with QA group. Requirements:  Ph.D. degree in Analytical Chemistry or related field with minimum of 1-3 years or MS degree with 3 to 7-years of bioanalytical experience in pharmaceutical industry.  Candidate must have first hand experience in bioanalysis that include instrumentation (LC/MS/MS, HPLC and liquid scintillation counting techniques), chromatography, solution chemistry, extraction techniques (e.g., SPE), automation (liquid handler, 96-well format), and electronic LIMS.  Candidate should have a broad knowledge in Good Laboratory Practices, drug development, PK and drug metabolism.  Candidate should have the ability to work in a project team environment, have excellent oral and written communication skills.  Good leadership skills are desirable. To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Sr. Project Coordinator/Group Leader, Clinical Packaging Pharmaceutical Research and Development Hauppauge, NY Description of Duties and Responsibilities: Manage partial day to day operations of department including but limited to the ones listed below  Oversee direct reports  Maintain department schedule and timelines  Maintain departmental data systems  Forecasting of product, resource and supply requirements  Project management: Oversee and schedule projects to be completed and ready to ship  Protocol Interpretation and breakdown.  Team Representation: Represent the CP dept. at team/R&D meetings to update and forecast the status of projects  Primary packaging: Package tablets, capsules, etc., into blisters & bottles  Clinical Labeling: Schedule and produce all labels required to complete packaging according to Medical, Regulatory and FDA requirements  Shipping and Returns: Schedule the shipping and returns of clinical materials to and from sites  Report and Protocol Writing: Create reports and documents to facilitate and record every aspect of all operations performed or projected  SOP creation, review and approval Requirements:  Bachelors Degree with 6-8 years of Clinical Packaging Experience (Clinical Label Experience desired)  Knowledge cGMPs and relevant FDA Regulations essential  Excellent communication and writing skills  High level of professionalism  Ability to prioritize, planning and problem-solving  Ability to handle multiple projects and work in a team environment To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Research Scientist to Principal Scientist, Exploratory Pharmaceutics Pharmaceutical Research and Development Farmingdale, NY Job Responsibilities:  Representing Exploratory Pharmaceutics in PR&D Core Development Teams.  Designing and conducting in vitro and/or in vivo studies that assist in the drug discovery and development.  Developing Bioavailability enhancers for poorly soluble compounds and evaluating alternative drug formulations and delivery technologies when optimizing bioavailability.  Be able to integrate the understanding of physiochemical and biopharmaceutical properties of drug compounds when assessing drug delivery systems.  Developing and using computational modeling system when evaluating drug delivery, absorption and bioavailability.  Maintaining Exploratory Pharmaceutics instrumentation (LC/MS/MS, in vitro lab)  Supervising chemists and /or Ph.D. scientist to conduct exploratory pharmaceutics activities Job Requirements/Education:  Ph.D. in Biopharmaceutics, Pharmaceutics, Pharmacokinetics or a related discipline with 2 - 10 years of relevant pharmaceutical industry experience.  Hands-on experience in analytical instrumentation (LC/MS/MS) and in vitro technique (bio-relevant dissolution, cell culture absorption models) is highly desirable.  Fundamental knowledge of formulation development, preformulation, drug delivery, pharmacokinetics and drug metabolism is necessary.  Good understanding of biopharmaceutical classification system (BSC) and In vitro / In vivo correlation (IVIVC) modeling is highly desirable.  Excellent verbal and written communication skills To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Research Scientist to Principal Scientist, Preformulation Pharmaceutical Research and Development Commack, NY Description of Duties and Responsibilities:  Conduct fundamental physico-chemical characterization of small drug molecules including pHsolubility profile, pKa, partition coefficients, polymorphism/salt screening, solid and solution state stability studies, etc  Conduct drug-excipient compatibility and other relevant studies to provide active support to formulators in the formulation development process  Conduct mechanical and thermal property evaluation on API and formulations using MDSC, TGA, DMA, texture analyzer and DCA  Perform experiments to monitor physical form change during pharmaceutical processing  Conduct solubility and multi-media dissolution studies to support BCS and in vitro/in vivo correlation  Develop oral and IV formulations to support in vivo PK, TK and pharmacological studies in animals  Supervise chemists and / or Ph.D. scientists to conduct the above preformulation activities Requirements:  Ph.D. in Physical Organic Chemistry/Pharmaceutical Chemistry/ Medicinal Chemistry/Analytical Chemistry/Pharmaceutics with 2-10 years experience in preformulation  Fundamental knowledge of pharmaceutical product development is a must  Training in analytical techniques and instrumentation such as HPLC, LC/MS, DSC, TGA, FTIR, HotStage Microscopy, Vapor Sorption, Isothermal Microcalorimetry, Particle Size Analysis and XRD is desirable  Expertise/Experience in thermal analytical testing is a plus  Knowledge of computer data sharing environment and a good understanding of formulations, especially solid dosage forms is necessary  Must be able to work in a team environment  Excellent verbal and written communication skills To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.

FOREST LABORATORIES
Named one of Fortune’s “Fastest Growing Companies” for three years running, Forest is an early to latestate developer that acquires compounds with potential and develops them into vital, marketable medicines. Lexapro, Aerobid, Tiazac, Namenda: Our focus is on therapeutic areas such as Central Nervous System, Cardiovascular, Pain Management, Pulmonary Respiration and Women’s Health. Our scientists develop new and innovative products that improve people’s lives every day. Join us in our unrelenting pursuit of pharmaceutical excellence, and be rewarded with a prominent role in Forest Research Institute’s crossfunctional R&D environment. Manager, Analytical Technology Transfer Quality Control Inwood, NY Description of Duties & Responsibilities:  Development/validation/transfer of analytical methods for release/stability testing of drug products  Development/validation of analytical methods for the detection and quantification of API residues in cleaning swab samples  Assist with the writing/reviewing/approving of analytical methods, validation protocols and reports.  Evaluations of analytical methodologies for legacy products and updating/(re) validating as needed to facilitate increased level of GMP compliance Position Requirements:  Ph.D. in Chemistry with a minimum of 5 years experience in the development/validation/transfer of analytical methods in a pharmaceutical laboratory  Strong background in HPLC and GC (packed and capillary column techniques)  Knowledge of Turbochrom/Totalchrom software  Knowledgeable in laboratory cGMPs  Effective technical communication skills  Ability to work in a fast paced environment To apply, please send information to: Forest Laboratories, Inc. Human Resources Department 500 Commack Road Commack, NY 11725 Fax: (631) 462-2794 e-mail: staffing_li@frx.com Please visit us on the Web at: www.frx.com Forest Laboratories is an Equal Opportunity Employer.


				
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Lingjuan Ma Lingjuan Ma
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