6 дней назад
Technical Associate
24 - 40$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Technical Associate (Solid Dose Pharmaceutical Manufacturing): Manufacturing and supporting tablet and capsule formulations for developmental, stability, and clinical supplies with an accent on cGMP compliance, equipment operation, and batch documentation. Focus on operating complex closed-transfer systems, investigating quality issues, calculating process metrics, and leading continuous improvement with Lean Manufacturing Techniques.
Location: On premise in Groton, Connecticut, United States; regular site presence, off-shift and weekend flexibility required.
Salary: $24.22–$40.36 per hour, plus potential overtime, weekend, holiday, and other pay premiums.
Company
develops and manufactures medicines and pharmaceutical products for patients worldwide.
What you will do
- Manufacture tablet and capsule solid dosage forms for developmental, stability, and clinical studies.
- Set up, operate, clean, and maintain complex pharmaceutical manufacturing equipment and closed-transfer systems.
- Prepare and execute batch records, logbooks, labels, electronic records, and in-process documentation.
- Support equipment lifecycle documentation, SOP creation and revision, quality reviews, investigations, and corrective actions.
- Perform operator care and maintain the cGMP manufacturing space.
- Lead continuous improvement projects using Lean Manufacturing Techniques and collaborate with Operations, Quality, Technical Support, and GWE.
Requirements
- High school diploma or GED.
- At least 2 years of cGMP experience in a biotechnology manufacturing or laboratory environment.
- Operational knowledge of computerized systems, production control systems, ERP systems, and other business applications.
- Strong Microsoft Office skills, especially Word and Excel, with excellent oral and written communication.
- Ability to work safely and effectively in a matrix team environment.
- Permanent authorization to work in the United States is required; visa sponsorship is not available.
Nice to have
- Bachelor’s degree.
- Knowledge of pharmaceutical solid-dose formulation, novel processing equipment, or commercial processing standards.
- Mechanical aptitude and willingness to perform hands-on manual work.
Culture & Benefits
- Safety, quality, compliance, teamwork, and continuous improvement are central to the work.
- Work involves standing, walking, bending, climbing, reaching, and lifting up to 55 pounds.
- Personal protective equipment, including gloves, a Tyvek suit, and respiratory protection, may be required.
- Benefits include a 401(k) with contributions, retirement savings contributions, paid vacation and holidays, caregiver, parental and medical leave, and medical, prescription, dental, and vision coverage.
- Relocation assistance may be available based on business needs and eligibility.
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