Supervisor Manufacturing Operations
Supervisor Manufacturing Operations
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Job Description
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Supervisor Manufacturing Operations Second Shift This position reports to our Minnetonka MN office
Welcome to an inspired career
At Halozyme we are reinventing the patient experience and building the future of drug delivery. We are passionate about the important work we do and we need innovative strategic problem solvers who drive business results by adopting the collective attitude necessary to make our ONE TEAM culture thrive. We embrace open honest and transparent communications to help us achieve collective win and we constantly strive to do more. Thats why we need youto help us make a significant impact by taking on increasingly complex challenges leaping beyond the status quo and advancing our mission.
Join us as a Supervisor Manufacturing Operations Second Shift and youll be part of a culture that welcomes diversity thinks differently to solve problems works collaboratively as one team and delivers meaningful innovations that impact peoples lives.
How you will make an impact
The Supervisor Manufacturing OperationsSecond Shift (This position will start with first shift and likely move to a 2nd shift in a few months. Hours for 2nd shift are 4:30pm 1:00am) leads a multishift production team of hourly and contract employees in the GMP manufacturing and packaging of pharmaceutical products at the Halozyme Minnesota Operations Facility. In this role you lead coach and mentor the manufacturing team on lean manufacturing and production standard processes to create a culture of engagement and continuous improvement while maintaining safety quality service and cost goals. Daily and line performance as well as strong leadership are vital for this position. The successful candidate will be familiar with best practices for cGMP assembly and packaging of combination pharmaceutical products in a cleanroom environment.
In this role youll have the opportunity to:
- Follow the requirements of cGMP ensure all manufacturing and packaging are performed following written procedures and reports infractions to Manager of Manufacturing Operations.
- Plan cleaning manufacturing packaging and documentation activities in a manner that enhances efficiency.
- Facilitate and partner with cross functional teams such as quality manufacturing engineering and product development to ensure coordination of activities.
- Assist with document/Batch Record review as subject matter expert.
- Promote safety quality and compliance amongst the team while maintaining Good Manufacturing Practices
- Identify manufacturing related issues perform root cause analysis and implement solutions as necessary.
- Communicate daily production activities and track performance against metrics to the Manager of Manufacturing Operations.
- Lead motivate and develop manufacturing technicians through engagement empowerment and collaboration.
- Monitor Quality Systems training for the Manufacturing Team. Assure assigned training is appropriate and completed on time.
- Identify training opportunities coaching and mentoring direct reports.
- Technical writing: create or modify documents utilizing change control and document revision systems to meet new or revised requirements.
To succeed in this role youll need:
- High School Diploma or equivalent with minimum of 5 years of experience working in a production environment (a combination of education and experience may be considered)
- Experience in the medical device or pharmaceutical industry preferred.
- Knowledge of Lean Manufacturing
- Experience with MS Office applications.
- Experience writing and reviewing technical documents and technical reports.
- Strong knowledge of Good Documentation (GDP) and current Good Manufacturing (GMP) Practices.
- Demonstrated experience in the training and development of employees in a manufacturing environment.
- Able to perform physical activity such as standing for long periods of time walking and working with hands.
- Background in industrial controls and PLCs.
- Associates Degree preferred.
In return we offer you:
- Full and comprehensive benefit program including an Employee Stock Purchase Program and 401(k) matching
- Opportunities to grow in a culture that prioritizes learning development and progression through inhouse programs and tuition reimbursement
- A collaborative innovative team that works as one to amplify your impacton your career the work you do and patients lives.
- This position requires you to work onsite full time
The most likely base pay range for this position is $83K $116K per year. Several factors such as experience tenure skills and particular business needs will determine an individuals exact level of compensation. Base salary is only one element of employee compensation at Halozyme. Total compensation could include bonuses sales incentives and equity awards.
Halozyme Inc. is an Equal Employment Opportunity (EEO) employer. It is the policy of the Company to provide equal employment opportunities to all qualified applicants without regard to race color religion sex sexual orientation gender identity national origin age protected veteran or disabled status or genetic information.
AccessibilityandReasonableAccommodations:
Halozyme is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans during our application process. If you need assistance or accommodation due to a disability contact Human Resources at .
To view all our open positions please visit our career page. Additionally our benefit offerings can be found here.
Required Experience:
Manager
Employment Type
Full-Time
