Qualifications
Responsibilities
Benefits
TITLE:
Production Supervisor - 2nd ShiftPOSITION OVERVIEW
The Production Supervisor role is responsible for safety, quality and performance of the prep, compounding filling area and inspection area. Will be working in an aseptic and non-aseptic area. The role will plan and coordinate all aspects of the production area.
HOW YOU9LL MAKE AN IMPACT
The responsibilities of this role include, but are not limited to, the following:
Oversee that operational areas are in cGMP compliance, and responsible for establishing systems that support the continuous improvement of procedures to heighten quality.
Ensures the timely and accurate documentation and closeout of batch records.
Manage the day-to-day activities of the operational area.
Develop and review SOPs pertaining to Prep, Compounding and Filling.
Drive continued improvement in operational areas.
Trend and take appropriate actions to agreed KPI.
People development and management.
WHAT YOU9LL BRING
Demonstrated leadership and supervisory skills
Minimum five (5) years of experience in a regulated industry
Minimum three (3) years related experience supervision is preferred
Experience in cGMP manufacturing or clean room production environment is preferred
Pre-filled syringe experience preferred
Ability to apply analytical reasoning and root cause analysis to solve problems
Strong math and calculating skills
Computer skills
Ability to read, understand, interpret and implement technical writing and instruction as well as have exceptional ability to solve problems in a fast-paced environment
Get certified on all the curriculums in the operational area to 1, understand the process and help to improve it. 2. Help to cover breaks, vacancies etc
Lead cross functional teams to solve urgent production issues, implement improvements
Work with operational team to improve KPIs or other trends/tasks independently
Independently investigate pharmaceutical operations and facility nonconformances, identifying any deviations from standards. This includes clearly defining problems, collecting, and organizing existing data, comparing causes to facts, identifying probable root causes, conducting interviews and SME discussions, and determining the best solutions for improvement of manufacturing processes, standard operations procedures (SOPs)and supply chain business practices
Review supporting documentation including batch documentation, ancillary documentation, test results / CoAs, product specifications, training records, SOPs, calibration records, packaging and validation protocols, and other technical documents
Assist with deviation/CAPA investigation and understand the process so if needed be able to take over and finalize an investigation/CAPA
Assist with revision to SOPs pertaining as an SME in the operating area
Be the SME during internal/external audits, lead presentations and present to the auditing team
Lead Tier 1 meeting and participate in Tier 2 meeting
Build a self-sufficient team that can work independently and have very little overview
Cover for peers and manager if needed
HOW WE INVEST IN OUR PEOPLE
Indivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do.The Indivior experience includes:
Pursuant to various state Fair Pay Acts, below is a summary of compensation elements for this role at the company. The following benefits are provided by Indivior, subject to eligibility requirements.
Starting Salary:$100,000-$115,000 USD
*Note actual salary is based on qualifications and experience
Our team will look into this right away.
