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- San Diego, CA

Our client - a major Pharmaceutical company in SoCal - is looking for Analytical Chemists. These Chemists will work within the company's Analytical R&D department. Responsibilities will include:Method Development / Method ValidationDevelopment of stability studies Performing literature searches Documenting/Recording all experimental activities in laboratory notebooksThe Qualified Candidate will have analytical methods development experience in a pharmaceutical environment. (4-10+....


Our client - a Pharma company in Central NJ - is looking for someone with strong experience with scale-up/tech transfer of sterile dosage forms (ideally Parenterals). In addition to having strong technical skills - the Qualified Candidate will have good “soft skills” since they will also be interfacing with CMOs. The Company said that they can fill this position at either a Manager or Sr. Manager level. This position requires BS in Chemical Engineering, Physical or Analytical Science or....


Our client - a growing Pharmaceutical company in Philadelphia is looking for Formulation Scientists. These are newly created positions. The Qualified candidate will have 3-12+ Years of Pharmaceutical experience primarily in the formulation of Solid Dosage Forms (IR/MR/ER). Experience with additional Dosage Forms is a strong plus. Additional responsibilities will include Report Writing (e.g. Product Development Reports, Submission Batch Reports etc.)

- Bedminster, NJ

A growing Pharmaceutical company in the Bedminster, NJ area, is looking for an Associate Director QA - CMC. This person will be responsible for ensuring CMC QA document review and approvals are performed in a manner that supports clinical release, regulatory approval, and commercialization of the company’s drug product programs. This person will be responsible for support of the following functional areas: Analytical Manufacturing Microbiology This person will also have responsibility for....


Our client, a major Pharmaceutical Company in the Central NJ area, is looking for a Sr. Mgr./Associate Director - Regulatory Affairs. The Sr. Mgr./Associate Director Regulatory Affairs will oversee a variety of projects (IND/NDA/BLA), and they will manage these projects through all phases of development as well as be involved with both post-approval and life-cycle management issues. The Sr. Mgr./Associate Director Regulatory Affairs will:Develop regulatory strategiesProvide regulatory....


Our client, a growing Pharmaceutical Company located in the Metro NY area, is looking for a QA Manager. The QA Manager will be responsible for:QA oversight of components, in-process and finished products etc.Hiring and training of all QA Inspectors & QA Reviewers.Overseeing work performance of all QA Inspectors & QA Reviewers.Ensuring cGMP and FDA complianceMonitoring and supporting quality systems such as laboratory investigations, deviation management, CAPAs, instrument....


Our client, a Pharmaceutical Company in Branchburg, NJ that is experiencing rapid growth, is looking for a Manager - Clinical Operations. The Manager will oversee clinical studies for compounds in variety of therapeutic areas. This position will be involved in developing study plans as well as helping to craft study budgets. Additional responsibilities will include CRO site selection as well as overseeing the CRO site qualification. The Manager will ensure that the clinical studies adhere to....


Our client, a Major Global Pharmaceutical Company, is actively expanding their operations in the U.S. They are currently looking for a Manager/Sr. Manager, Regulatory Affairs. The Manager/Sr. Manager will be responsible for submissions (IND/NDA/BLA) from Cradle to Grave - as well as the development and execution of global regulatory strategies. The ideal Candidate will also have some direct experience communicating with the FDA and various other Global Health Authorities. Additionally the....


Our client - a growing Pharmaceutical company in Raritan, NJ is looking for a Manager - Regulatory Operations. The Manager - Regulatory Operations will be responsible for development and implementation of procedures and systems to support Regulatory Submissions and Regulatory Publishing. The Manager will also be responsible for the establishment and maintenance of an archiving/document management systems and tools (e.g. eDMS, Regulatory Information System, CTD templates, etc.). The Manager....


Our client, a major Pharmaceutical Company in the Central NJ area, is looking for a Mgr./Sr. Mgr. - Regulatory Affairs. The Mgr./Sr. Mgr. - Regulatory Affairs will oversee a variety of projects, and they will manage these projects through all phases of development as well as be involved with both post-approval and life-cycle management issues. The Mgr./Sr. Mgr. - Regulatory Affairs will:Develop regulatory strategiesProvide regulatory guidanceReview documents for submission to FDAOversee the....

- St. Louis, MO

Our client - a major Pharmaceutical company in St. Louis - is looking for a Manager of Validation. The Manager will have overall responsibility for Validation in the following areas: Equipment Cleaning Packaging Process The Manager will be responsible for:Developing and implementing SOPs, Master Plans, Protocols for all of the above listed areas.Ensuring that all Plans and Protocols are compliant with both Company as well as External (i.e. FDA) requirements.Participating in Investigations and....


Our Client is looking for a Director - Technical Operations. This position is an outstanding opportunity to join a rapidly growing Pharmaceutical Company. This role will have a high level of visibility and will interact with both internal groups within the Company as well as external vendors. The Director will be responsible for:Overseeing multiple projects involving the Tech Transfer and Scale-up of Injectable Dosage FormsCollaborating with internal resources and vendors for all technical....

- Coram, NY

Our client, a rapidly expanding Pharmaceutical company located on Long Island, is looking for a QA Associate. The QA Associate will be responsible for a wide variety of responsibilities to include:Will be involved with document review, approval of protocols, approval of reports, lab investigations, batch record review, batch record release etc.Will work closely with & provide Quality support to R&D personnelWill assist in developing Quality SystemsWill assist in writing SOPs for....

- Morris Plains, NJ

Our Client, a major Laboratory Equipment Manufacturer, is looking for an Inside Sales Rep for their offices in Morris Plains, NJ This is a newly created position. The Company is looking for someone with a Biology or Chemistry degree - but no Sales experience is required. They are willing to train new employees for this role. This Company has been in business for over 105 years - and they continue to grow. The Inside Sales Rep will be responsible for: Telemarketing / Sales Activities Generating


Our client - a major Equipment/Appliance Manufacturer is looking for a Technical Support Specialist. The Technical Support Specialist will be responsible for providing phone and e-mail support to both end-users and dealers/distributors in order to resolve technical inquiries and technical issues with the Company’s products in a timely manner. They will also be responsible for maintaining records of these interactions according to the Company’s procedures. Additionally, they will escalate any....

- Raritan, NJ

Our Client, a Pharma Company in Piscataway NJ, is looking to add two Analytical R&D Chemists to their organization. These are newly created positions. This Company is continuing to expand. They are looking for Chemists with Method Development/ Method Validation/ Method Transfer experience. Ideally they would prefer Chemists with experience providing Analytical support for IND/NDA submissions. BS/MS Chemistry or related with 4+ yrs of Pharmaceutical Industry experience. HPLC, GC, Mass....

- Woodcliff Lake, NJ

Our client - a major Global Pharmaceutical company located in northern NJ - is looking for a Regulatory Operations Specialist. This position will be responsible for both Generic and Branded Products submissions. This Company's products include both Small Molecule as well as Large Molecule/Biologics products. The Regulatory Operations Specialist will be responsible for the following:Bookmarking and hyperlinking of regulatory documentation for submission to the FDA Quality control of images/....


Our client - a major Pharmaceutical Company is looking for a Project / Sr. Project Engineer. The Project / Sr. Project Engineer coordinates and provides engineering support for process improvement, planning, system design, capital expenditure requests, as well as the purchase, construction, alteration, installation, start-up and maintenance of both facilities and equipment. This position will afford the opportunity to make a direct impact at a company that is growing and will be significantly....

- Parsippany, NJ

QA Manager Our Client – a growing Pharmaceutical Company in Northern NJ – is looking for a QA Manager. The position will be responsible for the following: Overall cGMP complianceApproval and release of pilot, pivotal and commercial batchesReview and approval of batch manufacturing and packaging recordsReview, approval, and logs for Change Controls, Investigations of Deviations, Incidents, and OOS & OOTSampling of APIs, Finished products (including stability) and in-process samplesReview of

- East Hanover, NJ

Our client, a major Pharmaceutical company located in East Hanover, NJ is looking for a Director – Regulatory Affairs. The Director – Regulatory Affairs will be responsible for developing /implementing regulatory strategies as part of the Company’s Global Regulatory Affairs department. The Director will be the Lead Regulatory Strategist for the U.S. and will be the primary contact with the FDA. They will also be responsible for coordinating activities with both internal /external partners and....

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