Current jobs related to Contract Manufacturing Quality Associate - Highland Park - Sun Pharmaceutical Industries, Inc.
-
Manufacturing Associate
2 months ago
Oak Park, Illinois, United States Vault Manufacturing Full timePosition OverviewVault Manufacturing is seeking dedicated individuals for the role of Production Worker. This position is ideal for those with a passion for manufacturing and a desire to advance their careers within a stable organization.Available Shifts:Day Shift: Monday – Thursday 5 AM to 3 PM - $17.50/hrNight Shift: Monday – Thursday 5 PM to 3 AM -...
-
Manufacturing Technician II
4 weeks ago
Orchard Park, New York, United States Eaton Manufacturing Full timeJob Summary:Eaton Manufacturing is seeking a skilled Manufacturing Technician II to join our team. As a key member of our production team, you will be responsible for performing assembly and test processes on aerospace hardware.Key Responsibilities:Perform manufacturing processes on complex and routine assemblies under close supervision and follow standard...
-
Manufacturing Quality Engineer
5 months ago
Brooklyn Park, United States Cypress HCM Full timeA cutting-edge medical parts manufacturer in the Twin Cities is looking to bring on a direct hire, onsite Quality Engineer. This person will ideally come from Swiss Machining or Thermoplastics and will oversee all quality activities related to transfer of development activities, and manufacturing readiness, as well as ongoing support of design and...
-
Manufacturing Associate
4 weeks ago
Clifton Park, New York, United States Adecco Full timeJob OverviewAdecco is seeking a skilled Manufacturing Associate to join our team at Electronic Coating Technologies. As a key member of our production team, you will be responsible for safely operating automated processes, ensuring quality assurance standards are met, and maintaining a clean and organized work environment.ResponsibilitiesOperate automated...
-
Quality Assurance Auditor
1 week ago
Highland Park, New Jersey, United States Paragon Staffing, LLC Full timeJob DescriptionParagon Staffing, LLC is a company that specializes in connecting job seekers with employers who are seeking temporary, contract, or permanent positions.Job Summary:Quality Auditors oversee testing to ensure that products meet established standards of appearance or performance. Conducting hourly inspections on parts to ensure conformity and...
-
Quality Assurance Auditor
4 weeks ago
Highland Park, United States Paragon Staffing, LLC Full timeParagon Staffing, LLC is a company that specializes in connecting job seekers with employers who are seeking temporary, contract, or permanent positions. Due to the growth, Paragon Staffing, LLC is looking for Quality Assurance Auditors to join our team! Summary: Quality Auditors oversee testing to ensure that products meet the established standards of...
-
Manufacturing Process Engineer
2 weeks ago
Highland Park, Illinois, United States Shively Diversified Management Services Full timeManufacturing Engineer Job DescriptionWe are seeking an experienced manufacturing engineer to join our team at Shively Diversified Management Services. As a manufacturing engineer, you will play a critical role in enhancing and refining the automotive manufacturing process.Key Responsibilities:Analyze powertrain part prints and identify features and...
-
Manufacturing Quality Engineer
3 weeks ago
Overland Park, Kansas, United States Belcan Full timeJob Title: Senior Manufacturing and Quality EngineerLocation: Park City, UTEmployment Type: Full-Time, Direct Hire with Full BenefitsSalary Range: $/hour#AerospaceEngineering #QualityEngineering #ManufacturingExcellencePosition Overview:We are seeking an experienced Senior Manufacturing and Quality Engineer to optimize manufacturing processes and ensure...
-
Manufacturing Associate
1 week ago
Clifton Park, New York, United States Adecco Full timeJob OverviewElectronic Coating Technologies is seeking a skilled Manufacturing Associate to join their team. As a key member of the production team, you will be responsible for safely operating automated processes, ensuring quality assurance standards are met, and maintaining a clean and organized work environment. Key Responsibilities:Operate and maintain...
-
Manufacturing Associate
1 month ago
Clifton Park, United States Adecco Full timeJob DescriptionJob DescriptionNow hiring for a Manufacturing Associate at Electronic Coating Technologies! Weekly pay starts at 17.00 per hour, with first shift available. In this role, you will safely run automated processes, seek quality assurance feedback, ensure ISO and ESD standard operating procedures are followed, log information into the MRP system,...
-
Manufacturing Quality Engineer
1 month ago
Park City, United States Belcan Full timeJob Title: Senior Manufacturing and Quality EngineerLocation: Park City, UT 84098Area Code: 435Employment Type: Full-Time, Direct Hire with Full BenefitsSalary Range: $45.00-55.00/hour#AerospaceEngineering #QualityEngineering #ManufacturingExcellencePosition Overview:We are seeking an experienced Senior Manufacturing and Quality Engineer to join our team in...
-
Manufacturing Quality Engineer
4 weeks ago
Overland Park, Kansas, United States Belcan Full timeJob Title:Senior Manufacturing and Quality EngineerLocation:Park City, UTEmployment Type:Full-Time, Direct Hire with Full BenefitsSalary Range:$ /hourPosition Overview:We are seeking an experienced Senior Manufacturing and Quality Engineer to optimize manufacturing processes and ensure top-notch quality standards in aerospace applications.Key...
-
Quality Assurance Specialist
3 days ago
Hot Springs National Park, Arkansas, United States Amtec Contract Full timeJob DescriptionAmtec Contract is seeking a highly organized and detail-oriented Quality Coordinator to join our team. As a Quality Coordinator, you will be responsible for performing general administrative tasks, including data entry, report management, and laboratory data analysis.Key Responsibilities:Enter backflow prevention test report data into the...
-
Manufacturing Quality Engineer
2 months ago
Park City, United States Belcan Full timeJob Title: Senior Manufacturing and Quality EngineerLocation: Park City, UT 84098Area Code: 435Employment Type: Full-Time, Direct Hire with Full BenefitsSalary Range: $45.00-55.00/hour#AerospaceEngineering #QualityEngineering #ManufacturingExcellencePosition Overview:We are seeking an experienced Senior Manufacturing and Quality Engineer to join our team in...
-
Manufacturing Quality Engineer
1 month ago
Park City, United States Belcan Full timeJob Title: Senior Manufacturing and Quality EngineerLocation: Park City, UT 84098Area Code: 435Employment Type: Full-Time, Direct Hire with Full BenefitsSalary Range: $45.00-55.00/hour#AerospaceEngineering #QualityEngineering #ManufacturingExcellencePosition Overview:We are seeking an experienced Senior Manufacturing and Quality Engineer to join our team in...
-
Manufacturing Process Specialist
3 days ago
Highland Park, Illinois, United States Shively Diversified Management Services Full timeWe are seeking a skilled Manufacturing Process Specialist to enhance and refine the automotive manufacturing process. As part of a vibrant and innovative team, you will contribute to projects ensuring production processes are followed and operating optimally.Key Responsibilities:Analyze powertrain part prints and identify features and dimensions produced...
-
Water Quality Specialist
7 days ago
Hot Springs National Park, Arkansas, United States Amtec Contract Full timeJob SummaryWe are seeking a highly organized and detail-oriented Water Quality Coordinator to join our team at Amtec Contract. In this role, you will be responsible for managing water quality laboratory reports, entering data into our CC&B database, and performing other administrative tasks as directed.Key Responsibilities:Enter backflow prevention test...
-
Manufacturing Associate
4 days ago
Huntington Park, California, United States Aerotek Full timeJob SummaryAerotek is seeking a skilled Manufacturing Associate to join our team in Huntington Park. As a key member of our production team, you will be responsible for operating heavy machinery and performing various tasks to ensure the efficient production of high-quality products.Key Responsibilities:Operate heavy machinery, including electric welded...
-
Quality Associate
4 weeks ago
Hanover Park, United States Innova Solutions Full timeInnova Solutions has a client that is immediately hiring for a Quality AssociatePosition type: Full-time Contract to HireDuration: 9 months contract to hireLocation: Hanover Park, ILAs a Quality Associate you will:
-
Quality Assurance Specialist
4 weeks ago
Brook Park, Ohio, United States TRIGO Global Quality Solutions Full timeJob Title: Quality Resident Liaison/Automotive RepresentativeTRIGO Global Quality Solutions is seeking a highly skilled Quality Resident Liaison/Automotive Representative to join our team.Job Summary:The Quality Resident Liaison/Automotive Representative will be responsible for ensuring customer satisfaction, providing technical support, and promoting the...
Contract Manufacturing Quality Associate
3 months ago
Contract Manufacturing Associate
Job Summary
Support Quality activities at Contract Manufacturing Organizations (CMO) by providing timely and effective quality oversight. Accomplish quality objectives by planning and evaluating project activities. Support may include operations and validation.
Area of Responsibility
Review of manufacturing and packaging records
Review certificate of analysis and Certificate of compliance
Ensure the release packages are ready prior to batch disposition
Review of QMS records submitted by CMO and monitoring (e.g. change controls/deviations, quality agreements but not limited to)
Manage and oversee complaint, change control, and variation-filing modules for CMO activity.
Actively participate in day to day meetings
Participate in the qualification process and support assigned CMO aligned with the Sun Pharma Quality Management Systems and provide reports as required.
Implement, report and monitor CMO Quality Metrics and ensure identification and implementation of improvements needed through routine CMO business review.
Implement and maintain Regional CMO data in the Global CMO database.
Ensure the Quality Assurance Agreements which are created and maintained according to Sun Pharma requirements, are regularly reviewed and followed.
Conduct review and approve batch release documentation.
Support significant quality issues associated with Drug Products or Medical Devices originating from assigned CMO (complaints, deviations, recalls, counterfeits and product tampering, stability failures, etc.) appropriately and in a timely fashion.
Maintain annual auditing program, participate in technical visits and/or audits, manage action plans and follow up on agreed upon CAPAs.
Manage and oversee complaint module for Ohm Site. Work Conditions:
Office Environment
Lab Environment
Manufacturing Environment
Environmental related to manufacturing/production environments:
Noise: Sufficient noise, either constant or intermittent, to cause marked distraction or possible injury to sense of hearing.
Fumes: Smoky or vaporous emissions, usually odorous, thrown off as the result of combustion or chemical reaction.
Odors: Unpleasant smells.
JOB DESCRIPTION
Gases: Examples include carbon monoxide and ozone.
Dust: Airborne particles of any kind, such as textile dust, wood, and silica. Physical Requirements:
While performing the duties of this job, the employee is regularly required to use hands to handle or feel and talk or hear. The employee is frequently required to stand, walk, sit, stoop, kneel, crouch, crawl, push, and bend.
Must be capable of bending and lifting, moving and/or carrying up to approximately 20 pounds.
Ability to navigate office, lab, and/or plant floor working environments, stands, ambulates, and reaches.
Must have the ability to wear applicable personal protective equipment utilized at the site, including but not limited to respirators, safety glasses/goggles, and safety shoes. Travel Estimate
Up to 10 % Education and Job Qualification
Minimum of a Bachelor’s degree in a scientific discipline; MS preferred.
Certified Quality Auditor (e.g. ASQ) certification preferred.
Expert skills related to investigations (e.g. Lean Six Sigma) Quality Agreements, and CMO management.
Ability to identify key priorities necessary for and be able to author/implement global policies and procedures.
Strong understanding of technical pharmaceutical processes as well as risk assessment and risk management fundamentals/tools.
Strong knowledge of cGMP, QA/QC and regulatory compliance (US, EU and other regulatory requirements).
Strong interpersonal and communication, both written and verbal, skills.
Good negotiation and influencing skills.
Operational knowledge of pharmaceutical processing and packaging operations.
Task oriented team plan who is able to manage multiple complex priorities and work in a cross-cultural working environment.
The requirement for English language proficiency for this job role is Intermediate-B1+ (comparable to Global CEFR Independent B1) level based on the Common European Framework of Reference for Languages (CEFR). Experience
Minimum of five (05) years of related experience in a cGMP environment, preferably in a project management capacity for pharmaceutical or biotechnology industries.
Experience in drug product sterile pharmaceutical/biologics manufacturing and QC is an asset.
Actual base compensation may vary based on a number of factors, including but not limited to geographical location and experience. In addition, this position is part of the Annual Performance Bonus Plan, and may be eligible for the Employees are eligible to participate in Company employee benefit programs which include medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; and the employee assistance program. Employees also receive various paid time off benefits, including vacation time and sick time.
The compensation and benefits described above are subject to the terms and conditions of any governing plans, policies, practices, agreements, or other materials or documents as in effect from time to time, including but not limited to terms and conditions regarding eligibility. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company, or individual department/team performance, and market factors.
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of the incumbent(s).
EEO Notice:
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Notice to Agency and Search Firm Representatives:
Sun Pharmaceuticals (Sun) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Sun employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Taro. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral
