Biopharmaceutical Manufacturing Associate

Job Description

Job Description

Location: Plainville, MA 02762| On-site

Pay Rate: $34.50/hr on W2

Type & Duration: Contract | 9 months

 

Work Schedule: 6:45pm to 7:15am (with 30 min lunch)

Flex 12 rotating
Week 1 – M, T, F, Sa
Week 2 – Su, W, Th

 

Full Job Description:

• Execute work instructions and apply job skills to complete assignments.
• Achieve full training status and assist in 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 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

PPE provided. No steel toes, but closed toed shoes, GMP environment regulations – no piercing, no polish

• Required Skills: 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 of 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.

 

\nCompany Description

About Indotronix
Indotronix has been providing staffing services to Fortune 500 companies and federal, state, and local government agencies for more than 38 years. We have recently been recognized as one of the largest staffing companies in the US by Staffing Industry Analysts. To learn more about us or to view additional job opportunities, please visit our website at: iic.com.

Company Description

About Indotronix\nIndotronix has been providing staffing services to Fortune 500 companies and federal, state, and local government agencies for more than 38 years. We have recently been recognized as one of the largest staffing companies in the US by Staffing Industry Analysts. To learn more about us or to view additional job opportunities, please visit our website at: iic.com.