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Illumina

Supervisor, Manufacturing

Posted 3 Days Ago
Be an Early Applicant
In-Office
Woodlands, SGP
Entry level
In-Office
Woodlands, SGP
Entry level
Supervise production personnel in a biotechnology manufacturing environment, ensuring production goals are met and managing resources and talent development.
The summary above was generated by AI
What if the work you did every day could impact the lives of people you know? Or all of humanity?

At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.

Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible.

Position Summary

This position will provide effective leadership and supervision for production personnel on a high throughput biotechnology production line.

Position Responsibilities:

  • Oversee production in one or more of the following areas: reagent manufacturing, array, flowcell, manifolds production
  • Ensure production goals are met
  • Schedule and manage resources, track and report results, troubleshoot issues, train employees, and implement process improvements
  • Coordinate with Quality, Engineering, Shipping, and Planning groups to deliver results
  • Write and revise work instructions, and train technicians on the proper use of these documents
  • Responsible for efficient processing of work orders, reviewing batch records, maintaining training records, facilitating efficient shift changeovers, revision of work instructions, production scheduling and reviewing timesheets
  • Talent Acquisition activities which include identifying needs of the department, justification for budget to fill positions, coordinating with HR to market the position, review resumes, conduct interviews and identify and recommend a candidate as the potential hire, and employee orientation to the department and company.
  • Talent Development activities which include developing training plans with employees to ensure they have the necessary expertise to successfully perform their jobs, provide ongoing guidance to employees, and career counseling to help employees develop and advance in their careers
  • Job Role Definition ensures that job descriptions accurately record the primary responsibilities, qualifications and terms for each job role in their group
  • Performance Management activities include setting performance standards, ensuring employees have appropriate and realistic job goals, providing ongoing feedback about employees’ performance, conducting performance appraisals, including assessing how the employees have performed and how they can improve their performance, developing performance improvement plans if employees’ performance is not adequate and providing rewards for employee accomplishments.
  • Ensure employees follow all applicable company policies and procedures 
  • Other duties as may be determined by Management.

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.

Requirements:

  • Diploma or equivalent studies required; Bachelor's Degree or equivalent preferred
  • 0-3 years’ experience in a manufacturing environment, preferably with 1-2 years of supervisory experience
  • Experience with cGMP, ISO 13485, ISO 9001 operations is required
  • Candidates with night shift and/or 24/7 management experience will be highly preferred
  • Experience in inventory control, SAP or similar
  • Experience with hazardous chemicals is a plus
  • Excellent communication, leadership and interpersonal skills
  • Pharmaceutical / Life Science product manufacturing experience is preferred
  • Preference given to those with a command of GMP regulations as they pertain to clinical diagnostic products and expertise in transitioning processes from R&D to a manufacturing setting


We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact [email protected]. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.

Top Skills

Cgmp
Iso 13485
Iso 9001
SAP

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