Production Supervisor
Company: Aerotek
Location: Ledgewood
Posted on: February 23, 2021
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Job Description:
Description: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.Skills:Production, Supervision, Production
managementTop 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
suitAdditional 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 initiativeExperience 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
Aerotek.com.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.
Keywords: Aerotek, Newark , Production Supervisor, Other , Ledgewood, New Jersey
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