Hygiena provides rapid microbiology diagnostic tests and solutions for mission-critical, time-sensitive processes around the world. Hygiena’s proprietary diagnostic technologies enable customers to; prevent illness and save lives, comply with regulations, protect products and brands, run businesses more effectively. Solutions are sold in a wide range of industries globally, but the core focus is food safety. Headquartered in Camarillo, California and with offices around the world, we are actively looking for talented individuals to help grow the business!

At Hygiena we believe:

• In providing the highest quality products & service
• Being a leader in innovation
• Having a compelling desire to improve and win in the marketplace
• In contributing positively not only in the workplace, but in our community and environment!

With rapid growth comes opportunity. We are looking for a Laboratory Production Supervisor to join our team onsite in Camarillo! This is a full-time, exempt position.

Responsibilities:

• Manufactures all solutions per established SOPs, performs all required in-process testing, provides samples to Reagent Production Testing Group and coordinates with group to perform further in-process testing as required before it can be released to Production Manufacturing to fill according to schedule as determined by Master Scheduler Coordinates the status of the reagent manufacturing activities with production management and planning to ensure timelines for tasks and projects are scheduled to meet required timelines.
• Responsible for preparing, protecting, and troubleshooting any unforeseen performance issues on all chemical reagents and solutions as required to ensure product integrity and quality, performance from start to finish of the manufacturing process, including proper documentation (i.e., NCRs, Deviations, CoA). Provides technical support to the manufacturing team to ensure that the reagents and equipment required are ready to support the next phase of the manufacturing process. Responsible for ensuring processes are optimized and meet regulatory requirements and that tasks are executed by team as per established schedules.
• Participates in a variety of production activities to ensure product quality and promote continuous process improvements; these activities include projects, experiments, studies, aimed to investigate the impacts of an alternative chemical vendor source, certificate of analysis of new vendor lot of reagents, or collaborating on a new product development for new customers. Modifies and improves the outline of qualification processes to improve quality performance, ascertain critical QC specifications, and efficiency in procedures. Partners with Research & Development team to resolve product issues.
• Responsible for overseeing and conducting maintenance of the laboratory, equipment, and chemical reagents which is then documented as part of the established procedures to protect, prevent contamination, and ensure the safety of all personnel working in the area. Clearly communicates what is expected as part of molecular assay process, then verifies to ensure appropriate procedures have been followed.
• Oversees team of Laboratory Associates, establishing schedule, conducting regular meetings to ensure everyone comprehends responsibilities. Provides training as required for each team member and documents the training and provides copies to Document Control. Responsible for performance management, developing measurable key objectives/targets and provides support and guidance as needed. Ensure that all team members are trained in related procedures and operate in compliance with the work instructions and procedures.

Qualifications:

• Bachelor’s Degree in Molecular Biology, Microbiology, Biochemistry, Chemistry or a related scientific field or equivalent education and work experience required.
• Minimum of five (5) years of experience working in a biotechnology laboratory or manufacturing industry required that includes knowledge of cGMP, aseptic technique, attention to detail and includes the following:
  • Working in an ISO 9001 or 13485 compliant Quality Management system.
  • Experience with process control changes, root-cause investigation, non-conformance & deviation reports, implementation of corrective & preventative actions (CAPAs).
  • Hands on technical experience with molecular and microbiological techniques, including:
    • Polymerase Chain Reaction (PCR)
    • Southern Blotting.
    • Manufacturing of chemical reagents and solutions.
• Prior supervisory, leadership, and management experience required.
• Intermediate knowledge of Microsoft Office (Outlook, Word, Excel, Visio, PowerPoint) and Adobe Acrobat required.

Salary Range (applicable to California):

$80,000 - $95,000 base salary DOE

Supervisory Responsibilities:

In accordance with applicable policies/procedures and Federal/State laws, may perform the following supervisory responsibilities:   Interviewing, hiring orienting and training employees; planning, assigning, and directing work; coaching and appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems; enforcing all safety rules and ensuring safe work procedures.

Skills/Abilities:

• Comfortable with interacting and working with all levels of customers, both internal and external; good interpersonal skills, team motivation and outgoing personality
• Excellent adaptability in a fast-paced environment with the flexibility and willingness to take on new tasks and projects
• Ability to speak and write clearly and accurately
• Attention to detail and accuracy
• Effective listening skills
• Multi-tasking capabilities
• Must have in-depth analytical and problem-solving skills.
• Must be able to use discretion and independent judgement.

Working Conditions:

• Is required to work normal office hours (with some flexibility as per the below) Monday through Friday in the Office
• May occasionally work early morning/evenings/weekends to accommodate urgent customer requests in different time zones

Why you’ll want to join our team:

Teamwork as a core value.

At Hygiena, our emphasis on teamwork and cross-functional communication enables us to build stronger bonds within our business.

Be a part of something big.

Hygiena plays a critical role in helping to prevent global health crisis such as foodborne illness, healthcare-associated infections, and other outbreaks.

Giving back to our communities.

Hygiena believes in giving back by supporting local organizations committed to improving the lives of children and youth in our communities.

Benefits and Perks: 

• 15 days of PTO & 9 paid company holidays
• Medical with HSA employer contribution, Dental, Vision available 1^st of the month after start date
• Company paid Life Insurance, Short* and Long-Term Disability and an Employee Assistance Program
• 401(k) with Safe Harbor and Profit-Sharing employer contributions
• Tuition Reimbursement program
• Charitable Contribution matching
• Employee Referral bonus opportunities

*State paid short-term disability for California based employees

We are an equal opportunity employer and value diversity. All employment is decided on the basis of qualifications, merit and business need. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.