3 дня назад
Technical Associate, Clinical Manufacturing (Biotechnology)
24 - 40$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Technical Associate, Clinical Manufacturing (Biotechnology): Operating and documenting solid dosage pharmaceutical manufacturing processes and complex production equipment with an accent on cGMP compliance, continuous manufacturing, and cross-functional coordination. Focus on executing batch records, performing operator care, applying root cause analysis, and solving routine process and equipment problems in a clinical manufacturing environment.
Location: Onsite in Andover, Massachusetts, United States. Nights and weekends may be required based on process needs. Relocation assistance may be available based on business needs and eligibility.
Salary: $24.22–$40.36 per hour, with potential overtime, weekend, holiday, and other pay premiums.
Company
develops and manufactures medicines, with this role supporting clinical pharmaceutical manufacturing operations.
What you will do
- Execute solid dosage manufacturing activities within continuous manufacturing and PCMM work streams.
- Follow cGMP and safe handling procedures for pharmaceutical production.
- Operate complex manufacturing equipment and perform associated operator care tasks.
- Generate, assist with, and execute batch records and in-process run sheet documentation.
- Identify and resolve moderately routine problems while ensuring accuracy, quality, and procedural compliance.
- Coordinate with tech transfer, quality, and engineering teams and support continuous improvement using root cause analysis tools.
Requirements
- High school diploma or GED with 2+ years of relevant experience.
- Experience in a biotechnology manufacturing or laboratory environment.
- Operational knowledge of computerized systems, production control systems, ERP systems, and other business systems.
- Ability to work effectively as a member of a matrix development team.
- Excellent oral and written communication skills and proficiency in Microsoft Office Suite.
- Permanent authorization to work in the United States by any employer is required; U.S. work visa sponsorship is not available.
Nice to have
- Knowledge of fermentation, downstream processing, and microbial upstream and downstream processes.
- Experience with cGMP production of Phase I/II clinical drug substances.
- Experience commissioning and qualifying process equipment.
- Strong problem-solving, organizational, and attention-to-detail skills.
- Familiarity with common AI tools and interest in applying them to improve productivity.
Culture & Benefits
- Collaborative work across manufacturing, tech transfer, quality, and engineering functions.
- Dynamic team environment with diverse perspectives.
- 401(k) with matching contributions and an additional retirement savings contribution.
- Paid vacation, holidays, personal days, caregiver/parental leave, and medical leave.
- Medical, prescription drug, dental, and vision coverage.
- Physical work environment requiring extended standing, stair climbing, and lifting up to 50 pounds.
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