- Perform raw material and component review to ensure correct quantities, labeling and visual appearance.
- Perform weight checks for incoming and dispensed materials ensuring compliance with established procedures. Operates scales including set-up, verification, leveling and challenging.
- Follow Master Batch Records for the packaging of MDIs dosage forms when required.
- Identify defects and report quality issues.
- Set up, operate, and clean in compliance with batch records and SOPs, packaging equipment.
- Clean and sanitize packaging equipment per SOPs.
- Complete accurate and timely documentation. Follow good documentation practices in accordance with cGMP.
- Perform in-process testing and inspections as required by Master Batch Record (weighing, visual inspection etc.).
- Effectively performs activities and applies knowledge in accordance with approved SOPs, company policies, regulatory requirements, schedules and provides technical expertise and direction to colleagues.
- Actively participate in Production team and Site communication meetings.
- Support GMP investigations and events.
- Contribute to Standard Operating Procedure (SOP) writing in technical area.
- Follow strict internal protocols and Standard Operating Procedures (SOPs) as well as following current Good Manufacturing Practices (cGMP), complying with legal regulations, monitoring environment.
- Bachelor's degree in pharmaceutical engineering, Pharmaceutical Sciences or related field of study from an accredited college/university required.
- Master's degree in Pharmaceutical Engineering, Pharmaceutical Sciences, or related field of study from an accredited college/university preferred.
- 3 years of direct work experience in pharmaceutical manufacturing.
- 2-3 years of supervisory experience
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
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Nigh Shift Production Supervisor - Fall River, United States - Actalent
Description
We are seeking a Night Shift Production Supervisor with experience in pharmaceutical manufacturing to join our expanding company.
Schedule:
Monday - Friday, 11:00pm - 7:30am
Description:
Skills:
production management, mdi, production supervision, tablet, gmp, capa, Initiate Deviations, sop, batch record
Additional Skills & Qualifications:
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
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