Biopharmaceutical Manufacturing Associate

Location: Plainville, MA - 02762

Duration: 12 months

Pay Rate: $28 / $34.50

Shift: 7am to 7pm (Rotating) / 6:45pm to 7:15am

Week 1 – M, T, F, Sa
Week 2 – Su, W, Th

Summary:

As a manufacturing associate with a moderate to high level of technical expertise and experience. They independently perform routine operations and may handle more complex tasks within their scope of training. Actively participates in the day-to-day operations of a cGMP-compliant manufacturing facility and may assist in troubleshooting and minor problem-solving.

· Execute work instructions and apply job skills to complete assignments.

· Achieve full training status and assist training staff.

· Work on semi-routine assignments, receiving instruction on new processes.

· Maintain inventory records and accurate batch records.

· Inspect finished products for adherence to specifications.

· Assist with batch record reconciliation and preventative maintenance tasks.

· Adhere to Quality Management Systems and assist with Nonconformance/CAPA closures.

· Identify and communicate items requiring escalation.

· Maintain a clean and safe work environment.

· Follow company policies including safety, training, GDP, and cleanroom gowning.

· Spend 90% of the time in manufacturing suites.

Education: High school diploma or equivalent required.

Required: Minimum of 1 year of work experience in manufacturing, operations, production, lab setting or related field

Preferred: Experience in a cGMP environment

· Technical expertise in biopharmaceutical manufacturing equipment, principles, and processes.

· Strong understanding of current GMP and safety standards.

· Ability to function in a dynamic environment and balance multiple priorities.

· Proficiency in learning new software and tools.

· Ability to make decisions for moderately complex GMP manufacturing activities with minimal to moderate supervision.

· Ability to recognize, understand, and respond to situations requiring further evaluation and report to senior operators or management.

· Effective written and verbal communication skills with peers, senior associates, and area management.

· Understanding operational documents for GMP compliance, accuracy, and completeness.

· Ability to safely perform activities to prevent releases, accidents, and injuries.

· Ability to aseptically gown and/or sterile gown as needed.

· Required to write, read, and review documentation for extended periods.

· Specific vision requirements: close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus.

· Regularly required to talk and hear; frequently required to sit and stand for extended periods.

· Occasionally required to lift, walk, use hands to finger, handle, or feel; reach with hands and arms; stoop, kneel, or crouch.

· Required to wear Personal Protective Equipment (PPE).

· Daily computer use.

· May work with dry ice, liquid nitrogen cryogenics, hazardous and infectious agents, and experience marked changes in temperature.

Indotronix, founded in 1986 in New York, is a leading provider of IT, Engineering, Clinical, Scientific, and Professional staffing solutions.
As part of the Indotronix Avani Group, the company serves Fortune 500 organizations across diverse industry verticals.
With decades of industry experience and long-standing client relationships, Indotronix is recognized as a trusted talent and consulting services partner.