Laboratory QC Technician

*Please note, this is a temp-to-hire opportunity*

• Location: Rocklin, CA
• Hours: 40 hours a week. Training starts on 1st shift but need someone flexible for 2nd shift if needed.

Under supervision, the Quality Control (QC) Technician performs laboratory activities in the QC lab including inventory tracking, ordering maintenance, bio burden, slide filling, and IHC; completes required tasks based on QC schedule needs and follows standard operating procedures (SOPs) involving basic laboratory techniques, calculations, material measurements, operation of laboratory equipment and record keeping as necessary; supports the day-to-day activities of the QC department while adhering to applicable
regulatory requirements, and local and global Quality Management System (QMS).

Essential Functions:

• Perform paperwork preparation, bioburden, and all basic laboratory tasks
• Track inventory levels and order materials as required
• Use local ERP system to accurately document work where required
• Stock area inventories on a daily, weekly, and monthly basis
• Maintain lab cleanliness in compliance with cGMP requirements
• Maintain records and keep inventory updated
• Escalate non-conforming products to management, and participate in investigation process
• Meet productivity standards and strive to increase productivity without sacrificing quality and safety
• Look for ways to improve and promote quality
• Demonstrate accuracy and thoroughness
• Manage time and priorities to meet deadlines
• Troubleshoot equipment problems
• Maintain knowledge of SOPs and GMP regulations and guidelines
• Maintain cGMP compliance
• Participate on various projects to improve efficiency or compliance
• Maintain and demonstrate a high level of personal and professional integrity and report any suspicious activity

to laboratory management

• Respond promptly to customer needs, solicit customer feedback to improve service, meet commitments.
• Approach others in a tactful manner, react well under pressure, treat others with respect and consideration,

present a professional image in all business matters

• Meet productivity standards, strive to increase productivity without sacrificing quality and safety
• Look for ways to improve and promote quality; demonstrate accuracy and thoroughness
• Observe safety procedures, report potentially unsafe conditions, use equipment and materials properly
• Must be willing and able to work on weekends or extended hours as needed
• Follow regulatory and standard requirements as applicable to the site, i.e., MDSAP, ISO 13485, IVDR, and

compliance with the site Quality Manual.

• Other duties as assigned or required by the business

KNOWLEDGE, SKILLS & ABILITIES

• General knowledge of FDA QSRs cGMP, and ISO 13485 or other related industry standards is required
• Knowledge of FDA QSRs cGMP, and ISO 13485 or other related industry standards is preferred
• Knowledge of SAP and/or SAP NEXT preferred
• Good oral and written communication skills
• Good interpersonal skills
• Good documentation skills
• Good math skills: able to add, subtract, multiply, and divide in all units of measure, using whole numbers,

common fractions, and decimals; able to compute rate, ratio, and percentage

• Ability to read, analyze, and interpret instructions, correspondence, policies, procedures
• Ability to write reports, correspondence, and procedures

EDUCATION & EXPERIENCE:

• Minimum AA/AS degree in a biological science or related field is required
• BA/BS degree in biological science or equivalent life science degree is preferred
• Minimum two (2) years of experience in an FDA/ISO or other regulated environment is preferred
• Experience with calendaring, word processing, and spreadsheet software required; experience with

Microsoft 365 (Word, Excel, PowerPoint) preferred

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity. We believe that it drives excellence, innovation, and human progress. We care about our customers, patients, and our rich mix of people. This diversity strengthens our ability to lead in science and technology. We are committed to creating access and opportunities for all and empower you to fulfil your ambitions. Our diverse businesses offer various career moves to seek new horizons.

MilliporeSigma is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to his/her Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because he/she made a good faith report of discrimination.

Job Types: Full-time, Contract

Pay: $23.00 - $25.00 per hour

Expected hours: 40 per week

Schedule:

• 8 hour shift

Education:

• Associate (Required)

Experience:

• Laboratory: 1 year (Preferred)
• Pharmaceutical/ GMP industry: 1 year (Preferred)
• Quality Control: 1 year (Preferred)

Work Location: In person

Salary : $23 - $25