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Pharmaceutical jobs in Aspen Hill, MD

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Sr Manager, Clinical Process Quality
Rockville, MD
Job Purpose Responsible for implementing and manage clinical process quality oversight including QA review and approval for all SOPs covering GCP-regulated activities. QA responsible in process and related IT system change control in GCP regulated. Key Responsibilities: 1. Drive, coordinate and monitor implementation of new and revised GSK standards and policies ..

Last verified - 1 day(s) 11 hour(s) ago



Sr Manager, Clinical Development Quality Oversight
Rockville, MD 1 hit(s)
Basic qualifications: University degree or equivalent in Life Sciences. At least 8 years’ experience in the Pharmaceutical/biotech and/or contract research organization Experience and expert knowledge in the development process of new vaccines or other pharmaceuticals, preferable by having worked in different areas such as clinical development, clinical QA, technology development, project ..

Last verified - 1 day(s) 16 hour(s) ago



Clinical Country Operations - External Partnerships Lead
Rockville, MD
We are seeking a Clinical Country Operations-External Partnerships Lead for our new U.S. R&D Center in Rockville, Maryland. You will have the opportunity to be on the ground floor of a new organization and site, and you will be part of a new culture of some of the best scientific minds ..

Last verified - 1 day(s) 11 hour(s) ago



Expert Statistician
Rockville, MD
Support all aspects of non-clinical statistics in Technical Research & Development during product and process development, regulatory approval, technical transfer and commercialisation. Essential and accountable partner of project teams, management and key stakeholders in the organization in providing statistical support. Regularly develops new statistical concepts which are being applied in a ..

Last verified - 1 day(s) 11 hour(s) ago



Lead Biopharmaceutical Manufacturing Associate
Rockville, MD
Basic qualifications: BS/BA or Associates Degree, Degree in other discipline (or lack of degree) may be considered if sufficient technical depth has been achieved from professional experience 3-6 years prior manufacturing experience in the pharmaceutical or biotechnology industry Large Scale Purification experience preferred Experience working in a large scale cGMP Purification ..

Last verified - 1 day(s) 16 hour(s) ago


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Senior Mgr or Director, Clinical, Global Regulatory Affairs
Rockville, MD
•Provide support to the Global Regulatory Lead (GRL) for key regulatory activities pertaining to a project/product. • Interact with (or represents his/her area/product at) internal project related teams, for all parts of RA aspects of a given project on clinical RA strategy or procedural aspects. • Participate in project/product-related discussions and ..

Last verified - 1 day(s) 11 hour(s) ago



Lead Biopharmaceutical Manufacturing Associate
Rockville, MD
Why GSK? Because GSK’s Biopharm business vision is to leverage its experience and technical capabilities to launch, supply, and manage Biopharmaceutical products around the world. It will fulfill GSK’s Mission to Do More, Feel Better, and Live Longer by living its values: Integrity: Always doing the right thing; Commitment to the ..

Last verified - 1 day(s) 11 hour(s) ago



Clinical Research and Development Lead, RSV Maternal
Rockville, MD
Basic qualifications: MD or PhD with ability to independently research questions; sound scientific background required to critically evaluate all scientific aspects of vaccinology / immunology Minimum 3 years industry experience or minimum 10 years experience working in a scientific or medical institution (if not an MD, prior experience as Principal Investigator, ..

Last verified - 1 day(s) 16 hour(s) ago



Senior Regulatory Affairs Mgr
Rockville, MD
As the Senior Manager (Lead) –CMC, Global Regulatory Affairs, you will be leading regulatory Managers and/or Specialists in charge of the writing and edition of technical regulatory documents (CMC documents). These documents are needed to support development and registration of new vaccines, as well as to ensure maintenance of existing vaccine ..

Last verified - 1 day(s) 12 hour(s) ago



Pharmacist, GS-0660-13
Rockville, MD
Duties If selected for this position, you will support the audit, policy and pricing activities within the OPA to ensure compliance with statute, regulations, and established policy. Specifically, you will: Serve as authoritative consultant with direct interaction and communication with staff members, customers, and representatives from affected/interested entities on matters relating ..

Last verified - 1 day(s) 20 hour(s) ago


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