4 дня назад
API Manufacturing Associate I (Pharmaceutical Manufacturing)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
API Manufacturing Associate I (Pharmaceutical Manufacturing): Operating highly automated API manufacturing equipment and processes at a pharmaceutical production facility with an accent on GMP compliance, batch record review, and safe material handling. Focus on troubleshooting equipment, supporting qualification and validation activities, and maintaining production quality in clean-room and regulated environments.
Location: Clayton, North Carolina, United States; onsite pharmaceutical manufacturing facility
Company
is a global healthcare company producing medicines for diabetes, obesity, rare blood, and endocrine disorders.
What you will do
- Operate, monitor, and control highly automated API manufacturing processes and systems.
- Execute production schedules and load or unload products from trucks, tankers, and ISO containers.
- Review electronic batch records, SOPs, and GMP documentation in real time.
- Participate in qualification, validation, troubleshooting, equipment maintenance, and restoration of lost function.
- Maintain clean-room areas and perform environmental monitoring when required.
- Work safely and responsibly in accordance with site procedures and environmental requirements.
Requirements
- High school diploma or equivalent required; an associate degree or higher in technology, science, or engineering is preferred.
- Computer literacy, including operation of computer-driven manufacturing equipment and Microsoft Office.
- Ability to read and understand detailed product documentation and SOPs.
- Ability to perform material handling tasks and safely use material handling equipment.
- Ability to follow SOPs, safety guidelines, corporate and local regulations, and ISO standards.
- Ability to stand for up to 12-hour shifts, handle equipment or supplies weighing up to 33 pounds, work at heights or in confined spaces when required, and use protective equipment.
Nice to have
- At least two years of manufacturing experience in an FDA-regulated environment.
- BioWork or equivalent industrial, military, or vocational training combined with experience.
- Knowledge of cGMP pharmaceutical manufacturing, biology, chemistry, and mechanical systems.
- Experience with data-based troubleshooting, investigations, work permits, and Lock Out Tag Out systems.
Culture & Benefits
- Mentorship, career development resources, and opportunities to build manufacturing expertise.
- Fourteen paid holidays and generous paid time off.
- Health, dental, vision, life, and disability insurance effective from day one.
- Guaranteed 8% 401(k) contribution plus an individual company match option.
- Fourteen weeks of paid parental leave and six weeks of paid family medical leave.
- Tuition assistance, employee referral awards, and free access to -marketed pharmaceutical products.
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