Manufacturing Associate

Fladger Associates; Ridgefield (CT); On-site; USD 20,664 - 27,552; Full time

Job summary

A pharmaceutical manufacturing company in Ridgefield, CT is seeking an Entry-level Pilot Plant Operator. Responsibilities include assisting company technicians, maintaining safety standards, and participating in operational meetings. Ideal candidates are high school graduates or have an associate degree, with knowledge of GMP procedures and effective troubleshooting skills. The job offers a pay range of $15.00/hr to $20.00/hr and is contract-based.

Qualifications

• High School Graduate or Associate Degree required.
• Experience with GMP procedures and bulk manufacturing.
• Technical knowledge of manufacturing systems, methods, and procedures.

Responsibilities

• Follow the Lead of a Company Technician in pilot plant campaigns.
• Work with plant technicians and campaign managers to address challenges.
• Report all incidents to management and conduct operations with safety as the goal.

Skills

Effective troubleshooting skills with equipment and/or process

Understanding of GMP procedures

Proficiency in batch record entries and calculations

Education

High School Graduate or Associate Degree

Job description

Job posted 3 days ago. This range is provided by Fladger Associates. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range: $15.00/hr - $20.00/hr.

Responsibilities

• Excellent employment opportunity for a Pilot Plant Operator in the Ridgefield, CT area.
• Follow the Lead of a Company Technician in pilot plant campaigns.
• Work with plant technicians, campaign managers to address process and equipment related challenges.
• Assist the Company Lead technician in communication of the batch status with the chemist, Ch.D. analytical, MAS.
• Take all required training and complete before due date.
• Be involved in-group activities such as the 9:00 AM and 2:00 AM meetings.
• Become proficient in equipment operation, batch record entries, calculations.
• Attend PSOR Meetings, speak up and give input at these meetings.
• Follow all procedures, including the wearing of and use of defined PPE.
• Report all incidents, such as spills, exposures, cuts / abrasions etc. to management.
• Conduct all operations and activities with Safety as the #1 goal.

Experience

• High School Graduate or Associate Degree.
• Experience working with established GMP procedures and bulk manufacturing.
• Technical knowledge of manufacturing systems, methods and procedures.
• Possess effective troubleshooting skills with equipment and/or process.

Seniority Level

Entry level

Employment Type

Contract

Job Function

Research

Industries

Pharmaceutical Manufacturing, Biotechnology Research, and Food and Beverage Manufacturing

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