Shift: Hours: (Flexible on schedule) Monday to Friday
Job Descriptions
The contractor should have the following skills and qualifications:
Experience in technical/scientific writing to produce quickly and effectively concise, focused, understandable, accurate protocols, reports, emails, and other documents.
Strong and clear verbal and written communication skills.
Experienced in working with Microsoft Office programs such as MS Word and Excel.
Able to learn Heath Care digital information systems required to perform the role.
Must be able to work independently and to deliver on pre-defined project commitments.
Ability to manage several assignments simultaneously and be able to respond to the ever-changing needs of the various businesses.
Must be able to partner effectively with internal Central Stability and Analytical colleagues.
Stability, Analytical and/or scientific background, or experience is desired.
Ability to read, understand and follow applicable SOPs as written.
Knowledge of GMP regulations as they apply to drug products. Experience working in a GMP environment is a plus as the Health Care Sector is a regulated environment.
Alternatively, we are open to someone with experience in Project Management of GMP products. development (preferably FDA regulated). In this case, the contractor should have the following skills:
Managing CPS (critical path schedules) for drug products
Experienced and skilled in managing communication streams with multi-functional stakeholders (Technology Development, QA, Process and Formulation, etc.)
Comfortable driving clarity on dynamic timelines
Additional Information
At least 2 years of experience. Additional experience is welcome.
Understanding of Chemical Stability for Drug products
Technical Writing (MS Word and Excel)
Understanding of Global Boards of Health or at minimum FDA understanding.
Familiarity with the nature of work is a priority.
2-3 days of Work. Work will be queued for and will be based on the set deadline.
Education
Must have a BS (MS, PhD) degree and several years of experience in one or more of the following disciplines: analytical chemistry, organic chemistry, biochemistry, biology, microbiology, molecular biology/gene engineering, methods validation, pharmacology, NDA, quality assurance, quality control, report writing or calculations.
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Staffing and Recruiting
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