Supervisor Quality Control Job at Beacon Hill (Indianapolis)

Supervisor Quality Control

The Supervisor Quality Control is responsible for leading the Quality Control te...

Location

United States , Indianapolis

Salary:

85000.00 - 100000.00 USD / Year

Beacon Hill

Expiration Date

Until further notice

Requirements

Bachelor Degree in Chemistry, Science or related field required. Work experience is considered in lieu of degree
10 or more years of relevant experience required with previous supervisory experience preferred
Proficiency in cGMP laboratory testing and major laboratory instrumentation
Ability to interpret laboratory data and make sound compliance decisions based on such interpretations
Excellent communication and interpersonal skills
Ability to coach, mentor and teach
Excellent decision making, problem solving and analytical skills
Change agent with the ability to influence at all levels of the organization
Detail-oriented with the ability to work under tight deadlines
Ability to handle multiple priorities

Job Responsibility

Leading the Quality Control team to ensure compliance with all Corporate and local policies, procedures, and regulations
Scheduling laboratory testing and providing resource and instrumentation allocation
Conducting laboratory investigations
Implementing and monitoring corrective actions
Providing timely testing and notification of any aberrant occurrence to Management
Monitoring and maintaining quality programs that provide assurance for raw materials, components, finished products, intermediates, stability, and validation testing
Maintaining operational compliance with US and international regulatory agencies and guidelines (FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.)
Working cross functionally to coordinate testing schedules and communications
Performing testing as assigned
Scheduling and ensuring testing of production, raw materials, components, stability, validation, and support samples

Fulltime

Quality Control Supervisor

The Quality Control Supervisor is responsible for supervising the quality functi...

Location

United States , Winchester

Salary:

Not provided

Ardagh Group

Expiration Date

Until further notice

Requirements

High School Diploma or equivalent
Three years of experience in manufacturing quality
Must be able to handle multiple tasks in a team-based environment
Must have excellent presentation, interpersonal, and communication skills to interact effectively with management and outside customers
Must have excellent problem-solving, planning, and organizational skills
Must be proficient with Microsoft Office Suite

Job Responsibility

Assist and serve as back-up to the Quality Control Manager as directed
Interpret quality specifications and communicate to all applicable departments
Maintain all pertinent records to adequately monitor quality performance and standards
Review customer complaints with plant department to ensure corrective action measures are applied to prevent reoccurrence
Supervise ware audits and report findings along with recommended corrective action plans
Interact with customers and customer service representative to solve problems and foster strong customer relations
Oversee quality lab equipment calibrations and maintenance
Manage lab supply inventory and ordering
Manage the measuring of glass containers and provide reports
Perform activities necessary for the effective management of the quality department by training and developing unionized workforce

What we offer

Medical, prescription, dental and vision plans
Flexible Spending Accounts (FSA)
Life insurance
401(k) retirement plan with company match
Paid holidays and vacation
Short- and Long-Term Disability (STD/LTD)
Employee Assistance Program (EAP)
Apprenticeship programs
Professional and personal development opportunities through Employee Resource Groups

Fulltime

Quality Control Supervisor, Instruments

Quality Control Supervisor, Instrument - 2 will be responsible for: Provides dir...

Location

United States , Austin

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Life Science or Engineering discipline
5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree
8 years of relevant experience required with an Associate Degree
2 years of relevant Manufacturing Operations leadership experience

Job Responsibility

Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities
Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
Provides technical support and process improvement to minimize cost and increase productivity
Plays a key role in Lean Manufacturing Implementation
Supervises difficult inspection processes problems through a well and sound solution methodology
Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
Reviews inspection, labeling, and release logistic for appropriate process flow and documentation
Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
Oversees supplier quality metrics including but not limited to first pass yield
Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components

What we offer

Receive a competitive salary and benefits package as you grow your career at Diasorin

Fulltime

Incoming Quality Control Supervisor, Manufacturing

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutio...

Location

United States , Austin

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Life Science or Engineering discipline
5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree
8 years of relevant experience required with an Associate Degree
2 years of relevant Manufacturing Operations leadership experience

Job Responsibility

Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities
Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
Provides technical support and process improvement to minimize cost and increase productivity
Plays a key role in Lean Manufacturing Implementation
Supervises difficult inspection processes problems through a well and sound solution methodology
Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
Reviews inspection, labeling, and release logistic for appropriate process flow and documentation
Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
Oversees supplier quality metrics including but not limited to first pass yield
Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components

What we offer

competitive salary and benefits package

Fulltime

Quality Control Supervisor, Instruments

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutio...

Location

United States , Austin

Salary:

Not provided

Diasorin

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Life Science or Engineering discipline
5 years of relevant experience in a hardware manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree, preferred
8 years of relevant experience required with an Associate Degree, preferred
2 years of relevant Manufacturing Operations leadership experience, preferred

Job Responsibility

Provides direct supervision to the incoming inspection personnel and assures the effective use of all the resources to meet goals and requirements set forth by the Company and by Regulatory entities
Ensures Safety, Quality, GMP, ISO, and housekeeping standards are adhered to
Provides technical support and process improvement to minimize cost and increase productivity
Plays a key role in Lean Manufacturing Implementation
Supervises difficult inspection processes problems through a well and sound solution methodology
Ensures proper incoming inspection of components, packaging materials and final product in compliance with company procedures and ISO/FDA/GMP standards
Reviews inspection, labeling, and release logistic for appropriate process flow and documentation
Updates drawing, inspection procedures and any other documentation needed to inspect, test or purchase products
Oversees supplier quality metrics including but not limited to first pass yield
Collect and analyze data to track improvement and develop appropriate corrective actions, Conduct analysis, inspection, and trending in accordance with inspection plans work instructions and other quality standards to assure the quality of product or components

What we offer

competitive salary and benefits package

Fulltime

Quality Control Supervisor

Location

Canada , Knowlton

Salary:

Not provided

Randstad

Expiration Date

July 17, 2026

Requirements

A bachelor’s degree in chemistry, biochemistry, or a related field (or an internationally obtained degree with a recognized Canadian equivalency)
5–7 years of experience in a similar Quality Control Supervisor role or related capacity, ideally within a manufacturing or laboratory environment
A clear understanding of Data Integrity and ALCOA principles (Attributable, Legible, Contemporaneous, Original and Accurate)
Bilingualism (French and English) is essential, as the role involves frequent interactions with employees and clients
Strong interpersonal, communication, and coaching skills
Strong decision-making skills and the ability to demonstrate effective interdepartmental collaboration across the organization

Job Responsibility

Lead and empower: Manage the daily activities of the laboratory personnel responsible for testing raw materials, components, bulks, and finished goods, ensuring a seamless operational flow
Collaborate and solve: Act as the go-to Quality Control Supervisor, partnering daily with cross-functional departments to solve complex quality challenges and provide critical operational support
Champion quality investigations: Drive the Out of Specification (OOS) process by guiding your team through root-cause investigations, deviations, and non-conformities, while implementing sustainable CAPAs
Uphold rigorous standards: Ensure strict compliance with internal SOPs, GMP/GLP standards, and regulatory policies to maintain the highest benchmarks of quality
Invest in your people: Oversee the training, qualification, and competency of your staff, guaranteeing that the department is fully equipped and confident to operate across all shifts
Drive safety and sustainability: Cultivate a proactive Health & Safety environment through GEMBA walks and team reviews, while ensuring the environmentally responsible handling of hazardous materials

What we offer

A fun and dynamic environment that welcomes diversity in all its forms, talent, ideas, and creativity
Vacation: 3 weeks upon hiring
Comprehensive insurance including vision, dental, travel, and more
Short- and long-term disability insurance
Telemedicine/telepharmacy
RRSP: We contribute up to 4% of your salary, matching your contribution
Bonus: Access to a bonus program based on our success as a company and on your personal goals achieved
On-site cafeteria for convenient and pleasant lunch breaks
Internal mobility and career development opportunities to develop your potential

Fulltime

!

Quality Control Supervisor 2 (Reagents)

Assuming principal ownership of defined quality control sections and/or manufact...

Location

United States , Northbrook

Salary:

75000.00 - 100000.00 USD / Year

Diasorin

Expiration Date

Until further notice

Requirements

Associates of Science degree in the field of chemistry, biological sciences or related field degree Required
Bachelor of Science degree in the field of chemistry, biological sciences or related field degree, preferred
8+ years of Relevant experience in a manufacturing environment in an FDA regulated industry and/or ISO certified organization with an Associate's Degree
2+ years of Relevant Quality Operations leadership experience
5+ years of Relevant experience in a manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelor's Degree
Mathematics aptitude
Knowledge of clean/HEPA filtered manufacturing environments
Knowledge of purified water systems Low Statistical aptitude
ISO 13485 and FDA Quality Systems knowledge
Proficiency in use of process based Manufacturing Resource Planning systems such as Oracle or SAP

Job Responsibility

Deliver attainment of production schedule for finished product
Coordinate (development and implementation) the daily work schedule
Supervise associated quality control personnel
Establish and maintain appropriate role-specific training plans
Perform in-process quality control sampling and analytical testing
Deliver and ensure timely completion of process documentation
Investigate Out of Specifications
May oversee section cycle counts
May oversee the timely and accurate completion to support stability studies
May oversee specific calibration and maintenance of equipment and infrastructure

What we offer

health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks

Fulltime

Quality Control Supervisor

Why Valvoline Global Operations? At Valvoline Global Operations, we’re proud to ...

Location

United States , Cincinnati

Salary:

Not provided

Valvoline

Expiration Date

Until further notice

Requirements

4-year degree focused in Biology or Chemistry
Will consider engineering
Basic computer skills, Microsoft Office Suite
Experience in manufacturing environment
Experience in a lab setting
Experience working in LIM's and SAP
Must be authorized to work in the U.S.
Working Conditions / Physical Requirements: Ability to lift 50lbs, walk up and down stairs and move throughout the plant and office frequently

Job Responsibility

Review plant quality process and drive the continued improvement mindset
Oversight of the ISO 9001 certification and related auditing of facility processes
Drive lab safety and process compliance
Initiative to drive trouble shooting and root cause analysis (RCS's) for both internal and supplier issues
Linking corrective actions to process development
Helping build and maintain work instructions while improving process controls
Learn plant processes and support auditing against control plans and work instructions
Supporting lab tech training and development amongst peers
Support improvement projects tied to the lab and supplier quality
Manage lab supplies and consumables

What we offer

Health insurance plans (medical, dental, vision)
HSA and flexible spending accounts
401(k)
Incentive opportunity
Life insurance
Short and long-term disability insurance
Paid vacation and holidays
Employee Assistance Program
Employee discounts
Tuition reimbursement

Fulltime

Select Country

Supervisor Quality Control

Job Description

Job Responsibility

Requirements

Looking for more opportunities?

Supervisor Quality Control

Supervisor Quality Control

Quality Control Supervisor

Quality Control Supervisor, Instruments

Incoming Quality Control Supervisor, Manufacturing

Quality Control Supervisor, Instruments

Quality Control Supervisor

Quality Control Supervisor 2 (Reagents)

Quality Control Supervisor

Our AI answers in your language