Quality Control Manager

Yoh,-A-Day-; Noblesville (IN); On-site; USD 88,000 - 125,000; Full time

Benefits offered by this job

Medical benefits

Dental & Vision BENEFITS

401K Retirement Savings Plan

Health Savings Account (HSA)

Life & Disability Insurance

Direct Deposit & weekly epayroll

Referral Bonus Programs

Training opportunities

Job summary

Noblesville, Indiana-based Yoh is seeking a Night Shift Quality Control Manager for a pharmaceutical manufacturing client. The role runs Saturday through Wednesday, 4 am to 12:30 pm, and requires ensuring compliance with regulatory agencies, coordinating QC testing, and leading a quality team.

Ideal candidates will have a chemistry or science degree (or equivalent experience) and 7+ years in QC with supervisory background. Competitive salary and benefits offered by Yoh.

Qualifications

• Bachelor degree or higher in a science field; work experience may substitute.
• 7+ years of relevant experience with prior supervisory responsibilities.
• Proficiency in cgmp laboratory testing and major lab instrumentation.

Responsibilities

• Ensure regulatory compliance with US and international agencies (FDA, ISO, etc.).
• Coordinate testing schedules and QC activities with production teams.
• Perform testing and validate results for materials, components and stability.
• Maintain controlled documents and ensure 5S and cleanroom standards.
• Lead and develop the QC team to high performance and ownership.

Skills

Regulatory compliance

cGMP knowledge

Quality testing

Data interpretation

Supervisory experience

Education

Bachelor's degree in Chemistry, Science or related field

Tools

Laboratory instrumentation

Job description

Night Shift Quality Control Manager (BH-398613)

Location Noblesville, United States Sector Pharmaceuticals Salary $115,000.00 to $125,000.00 per annum

Yoh is hiring a Night Shift Quality Control Manager for our Pharmaceutical Manufacturing client in Noblesville, Indiana.

Saturday - Wednesday, 4 am - 12:30 pm.

Essential Job Functions

• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
• Work cross functionally to coordinate testing schedules and communications in support of the weekly production activities and ensure QC testing and maintenance activities are completed per requirements.
• Perform testing as assigned.
• Schedule and ensure testing of production, raw materials, components, stability, validation, and support of protocol/experimental samples.
• Verify, review, and make appropriate changes if needed, to any controlled document(s) pertinent to area of responsibility.
• Ensure team compliance with all policies, procedures, and site/company regulations.
• Support investigations of process or product failures and customer complaints. Author, and/or review all area quality and safety exceptions and investigation reports.
• Facilitate on time completion of all corrective action items assigned to area.
• Work safely with radioactivity and ensure all direct reports maintain radiological exposure to levels As Low As Reasonably Achievable (ALARA).
• Coach and develop the team to High Performance while fostering a culture of team ownership. Recognize and reward performance.
• Set clear vision by ensuring goals and objectives are aligned with site strategies and managing each team member's performance management.
• Provide leadership for employees through effective communication, coaching, training and development and provide solutions for the success of the team.
• Measure and communicate team progress against individual, team and site goals and Key Performance Indicators (KPI's).
• Manage the department overtime (OT) and ensure that all exception reports are completed and submitted as required.
• Maintain an acceptable level of 5S in the area and promote proper maintenance and cleanliness of the department areas of responsibility.
• Assure compliance with department training and qualification.

Requirements

• Bachelor Degree in Chemistry, Science or related field required. Work experience is considered in lieu of degree.
• 7 or more years of relevant experience required with previous supervisory experience required.
• Proficiency in cGMP laboratory testing and major laboratory instrumentation.
• Ability to interpret laboratory data and make sound compliance decisions based on such interpretations.

Estimated Min Rate: $87500.00

Estimated Max Rate: $125000.00

What's In It for You?

We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh's network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh's extensive talent community that will provide you with access to Yoh's vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

• Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)
• Health Savings Account (HSA) (for employees working 20+ hours per week)
• Life & Disability Insurance (for employees working 20+ hours per week)
• MetLife Voluntary Benefits
• Employee Assistance Program (EAP)
• 401K Retirement Savings Plan
• Direct Deposit & weekly epayroll
• Referral Bonus Programs
• Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. 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.

Visit https://www.yoh.com/applicants-with-disabilities to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.