Manufacturing Associate III - Visual Inspection and Packaging

Futureshaper.com; North Carolina; On-site; USD 10,000 - 60,000; Full time

Job summary

Join a forward-thinking company dedicated to delivering life-changing medicines as a Manufacturing Associate III. This role is vital in supporting processing steps and manufacturing activities, particularly in Parenteral Filling operations. You will work in a collaborative environment, ensuring compliance with cGMP standards and contributing to a mission that impacts lives. Ideal candidates are energetic and thrive in fast-paced settings, ready to embrace challenges and adapt to the complexities of biomanufacturing. This position offers competitive pay, comprehensive benefits, and opportunities for personal growth.

Benefits

bonuses

equity incentives

wellness programs

insurance

paid time off

parental leave

401(k) matching

tuition reimbursement

Employee Resource Groups participation

Qualifications

• Bachelor’s Degree or equivalent with relevant experience required.
• Visual inspection ability to detect small particles and imperfections.

Responsibilities

• Execute daily manufacturing activities and validate protocols.
• Document cGMP data and maintain clean work environment.
• Participate in training and development initiatives.

Skills

cGMP SOPs

team collaboration

investigation of procedural deviations

visual inspection

adaptability

Education

Bachelor’s Degree in STEM

BioWorks Certificate

High School Diploma

Job description

Manufacturing Associate III - Visual Inspection and Packaging

Research Triangle Park, NC, United States

Salary Range: $26-33.50 per hour

Job Description

This position involves working a four-day, ten-hour shift from 6 a.m. to 4 p.m., Monday to Thursday.

About This Role

Manufacturing Associates support processing steps and manufacturing activities at our Research Triangle Park facilities. These teams are vital to our operations, playing a critical role in delivering therapies to patients. This role focuses on our Parenteral Filling operations, with teams operating across various units.

Key Responsibilities

1. Execute daily manufacturing activities, including operating process equipment and validating protocols according to cGMP SOPs.
2. Document all cGMP data and information, including deviations, for processing steps and equipment activities. Create and update batch records, SLRs, and equipment logbooks.
3. Maintain a clean and safe work environment, ensuring audit readiness.
4. Contribute as a team player and leader, bringing energy and focus.
5. Assist in investigations of procedural deviations.
6. Adhere to aseptic gowning and operating procedures.
7. Participate in and lead training and development initiatives for personal and team growth.

Candidate Profile

Ideal candidates are passionate about contributing to life-saving missions, demonstrate learning agility, are energetic, and thrive in fast-paced environments. Flexibility and adaptability are essential due to the complex nature of biomanufacturing.

Qualifications

Required

• Bachelor’s Degree (preferably in STEM) with at least 6 months of relevant experience, or
• BioWorks Certificate or Associate’s Degree with at least 1 year of relevant experience, or
• High School Diploma (or equivalent) with at least 1.5 years of relevant experience.

Physical Requirements

• Visual inspection ability, confirmed through initial and annual exams, to detect small particles and imperfections.
• Ability to work 12-hour shifts on a rotating schedule.
• Ability to lift up to 25 pounds regularly and up to 50 pounds occasionally.
• Strong desire for quick learning and adaptability.

Additional Information

All personal information will be kept confidential per EEO guidelines.

The hourly pay range is $26-33.50, determined by skills, experience, location, and internal factors. Benefits include bonuses, equity incentives, wellness programs, insurance, paid time off, parental leave, 401(k) matching, tuition reimbursement, and participation in Employee Resource Groups.

Why Join Us?

We are committed to excellence, innovation, and inclusion, offering a collaborative environment where every role contributes to our mission of delivering life-changing medicines. We value diverse backgrounds and perspectives, fostering an inclusive culture where all employees feel empowered and inspired.

We consider all qualified applicants without discrimination based on gender, race, age, disability, or other protected categories. Biogen is an E-Verify Employer.