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Production Supervisor - 2nd SHIFT



Posting ID: JP-002026427

Full Time
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IMMEDIATE OPPORTUNITY - PRODUCTION SUPERVISOR IN PHARMA! This is a great time to join a growing pharmaceutical company as a Production Supervisor. This company is dedicated to delivering high-quality and innovative medicines to patients and provides opportunity for career growth. THIS IS A FULL TIME PERMANENT OPPORTUNITY (Mon-Fri).


The Production Supervisor directly leads the activities of the Operations in the Production area and is responsible for leading direct reports. The Production Supervisor ensures manufacturing, filling, inspection, packaging and labeling jobs are executed accurately with the highest quality, meet applicable cGMP requirements, and are completed on time per the production schedule. The Production Supervisor works with the highest degree of accountability and customer service to ensure client needs are met in a timely manner.

-Provides overall Leadership to the Sterile Production Team structured around:

-Leads Production team members by providing them strategic vision and direction aligned with Organization’s core values.

-Integrates and drives collaboration within the Sterile Production area to achieve highest levels of quality.

-Fosters and drives collaboration within the production area for improvements which will result in high quality products and customer satisfaction.

-Drives, implements and sustains changes to attain highest standards of performance.

-Facilitates communication and drives accountability.

-Provides a work environment that fosters positive energy, creativity and team work.

-Must be able to review and approve production batch records in a timely manner.

-Must be gown qualified to supervise production in the clean room.

-Supervise a one-shift operation by spending at least 50% of available time interfacing with employees to ensure that all batches are of high quality and exceed all the Company’s current Good Manufacturing Practices (CGMPs) and follow all safety guidelines.

-Ensure that production schedule is met by distributing workload in accordance with changing priorities by working in collaboration with Quality, Supply Chain, Engineering, Product Development and Maintenance departments.

-Ensure sterile production operations are properly controlled and regulatory compliance requirements are met by ensuring batch documentation is accurate, Standard Operating Procedures (SOP’s) are accurate and personnel training is current, critical documentation templates are accurate, equipment is in good repair and current calibration, and high standards of housekeeping are maintained in all areas of responsibility.

-Provide feedback for continuous improvement. Assist with hiring and disciplining staff, as required. Support the ---Company’s safety program to maximize safety awareness and provide a safe work environment.

-Evaluate /solve production problems by reviewing the area of concern, developing potential solutions, technically evaluating or testing the solutions, and preparing summary reports/recommendations for management.

-Supports continuous improvement by completing work on time, identifying potential issues, and driving to improve work processes and procedures relative to manufacturing and/or filling and packaging equipment.

-Write investigations and CAPA’s for non-conformances and deviations generated by the production departments. --Write and maintain SOPs and other manufacturing specifications.

-Develop and Monitor KPI’s to improve department metrics including scrap, non-conformance, batch record errors and plant efficiencies.


Production, Supervision, Production management

Top Skills Details:

Can work 2nd shift 3-11:30pm M-F

(training will be on first)

Experience with leading a team, working in a manufacturing environment, gowning in ISO 5 full bunny suit

Additional Skills & Qualifications:

Must have 3 - 5 years’ leadership experience in a cGMP regulated environment and have worked in a pharmaceutical, Biotechnology or medical device manufacturing facility.

Minimum of 3 - 5 years’ previous experience in a pharmaceutical manufacturing or medical device preferably in sterile environment.

Ability and willingness to work and participate effectively in a team environment.

Ability and willingness to maintain accurate and factual hard copy and electronic records.

Attention to detail, safety, quality and customer requirements.

Ability to effectively communicate verbally and in writing to subordinates, peers and management.

Ability to read information and apply what is described in the reading material to situations that may contain several details or describe processes involving several steps.

Demonstrate high level of personal motivation and initiative

Experience Level:

Intermediate Level

About Aerotek:

We know that a company's success starts with its employees. We also know that an individual's success starts with the right career opportunity. As a Best of Staffing® Client and Talent leader, Aerotek's people-focused approach yields competitive advantage for our clients and rewarding careers for our contract employees. Since 1983, Aerotek has grown to become a leader in recruiting and staffing services. With more than 250 non-franchised offices, Aerotek's 8,000 internal employees serve more than 300,000 contract employees and 18,000 clients every year. Aerotek is an Allegis Group company, the global leader in talent solutions. Learn more at

The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

Contact Information

Recruiter: Stephanie Cavico

Phone: (732) 447-1191


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