Supplier Quality Management Specialist

1 month ago

Boulder, United States Corden Pharma Boulder, Inc. Full time
EQUAL OPPORTUNITY EMPLOYER

Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.

CordenPharma is a leading full-service contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (APIs), excipients, and pharmaceuticals Drug Products (DP) and packaging capabilities with > 2,600 employees across the world. Our services enable pharmaceutical and biotech companies to manufacture medicines with the ultimate goal of improving people's lives.

Our network in Europe and the U.S. offers flexible and specialized solutions across five technology platforms: Peptides, Lipids, & Carbohydrates; Injectables; Highly Potent & Oncology; and Small Molecules. We strive for excellence in supporting this network and are committed to providing the highest quality products for the well-being of patients.

SUMMARY

Reporting into Quality Assurance and works cross functionally to execute and improve the Supplier Quality Management (SQM) Program and develop alignment across on all processes relating to Supplier Risk Management (SRM) for Corden Pharma Colorado (CPC), and Corden Pharma Boulder (CPB).

Responsible for:

  • Directing the management and enhancement of a phase-appropriate supplier qualification, using risk-based tools for qualification, classification, and monitoring
  • External supplier material performance, compliance, and reliable quality of materials that meet business and market requirements
  • Evaluating potential new sources of supply and selecting appropriate suppliers based on supplier assessment/audits, quality performance and systems, risk profile, and business/customer requirements
  • Keeping up to date on business intelligence, market trends, and changes in business practices in the CDMO landscape
  • The position will review, define, and monitor requirements for supplier quality management processes and supplier performance measurement, while adding value for our suppliers as partners
ESSENTIAL DUTIES AND RESPONSIBILITIES

Include the following. Other duties may be assigned.
  • Collaborate with Supply Chain, R&D, Process Engineering, Project Management, and Regulatory Affairs to define and execute a process for second sourcing raw materials
  • Responsible for identifying and prioritizing supplier audits including requirements for and performance of supplier audits; and issuance of reports and coordination of responses
  • Assures adherence to audit schedule, management of audit closure for suppliers of raw materials and components, and maintenance of the approved supplier list
  • Performs Qualification of new vendors and materials by gathering and evaluating specification information
  • Responsible for partnering with customers across site, key stakeholders, and management, to communicate/escalate and ensure timely and adequate management of quality risks
  • Monitors supplier quality and performance: Assess and report on supplier performance metrics for QMRs
  • Establishes and maintains a Supplier Relationship Management (SRM) process with continuous improvement goals/programs
  • Provides direction to team as Quality SME for supplier issues and discrepancies, and lead/manage the investigations to resolve the issues as warranted for significant matters. Resolve issues pertaining to damaged goods, late deliveries, quality issues, and contractual disagreements
  • Assures execution of the supplier-initiated change process is timely for processing of change impacts and coordination with Supply Chain to manage any inventory impacts
  • Collaborates cross-functionally and with the suppliers to improve partnerships and preparation for future growth
LEADERSHIP & BUDGET RESPONSIBILITIES

Provide leadership and harmonization for the management and improvement to the Supplier Quality Management Program across both Corden manufacturing sites.

SAFETY & ENVIRONMENTAL RESPONSIBILITIES

Every individual is personally responsible for the safety and environmental aspects of his or her activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.

QUALIFICATIONS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

EDUCATION and/or EXPERIENCE

Bachelor's degree (BS) with 10 years of related experience and/or training; or equivalent combination of education and experience, including experience in a Manufacturing Environment. Previous experience of Supplier Management and external Quality Auditing desirable, but not essential. Candidate should have a background working with SAP (or similar ERP system) and Microsoft Office Suite.

LANGUAGE SKILLS

Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of organization.

MATHEMATICAL SKILLS

Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.

REASONING ABILITY

Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

CERTIFICATES, LICENSES, REGISTRATIONS

CSQP/CSPC accreditation preferred and needed within 5 years of hiring date.

PHYSICAL DEMANDS

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to sit and work with hands. The employee frequently is required to talk or hear. The employee is occasionally required to stand and walk. The employee may occasionally lift and/or move up to 25 pounds.

WORK ENVIRONMENT

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts, fumes or airborne particles, and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate.

CORE COMPETENCIES

These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.
  • Relevant experience in pharmaceutical/biopharmaceutical/chemical/manufacturing processes and related Quality Assurance, Quality Auditing and Supplier Management
  • Strong working knowledge of cGMP, GLP, good clinical practices, FDA Guidelines and Points to Consider documents, and standards routinely used in the industry (ANSI, ISO, Federal Standards)
  • Strong analytical, organizational, and scheduling skills, and creative problem-solving skills
  • High level of interpersonal skills with strong negotiation skills and contract development experience
  • Proficient in computer systems such as word processing, spreadsheets, and ERP software packages (SAP)
  • Strong written and verbal communication, and presentation skills
  • High degree of business ethics
SALARY

Actual pay will be based on your skills and experience.

BENEFITS
  • 401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service
  • Accident Plan
  • Critical Illness Insurance
  • Dental Insurance
  • Disability Insurance
  • Employee Assistance Program
  • Flexible Spending Account
  • Health Insurance PPO/HSA
  • Hospital Indemnity Plan
  • ID Theft Protection
  • Life Insurance
  • Paid Maternity/Paternity Leave
  • Tuition Reimbursement
  • Wellness Program
  • Vacation - Three Weeks 1st Year
  • Vision Insurance

This Posting has been extended to October 5 2024.

  • Supplier Quality Assurance Specialist

    1 month ago

    Boulder, Colorado, United States Corden Pharma Boulder, Inc. Full time

    Job SummaryCorden Pharma Boulder, Inc. is seeking a highly skilled Supplier Quality Assurance Specialist to join our team. As a key member of our Quality Assurance department, you will be responsible for ensuring the quality of our suppliers and their products.Key ResponsibilitiesDevelop and implement supplier qualification and approval processes to ensure...

  • Quality Assurance Specialist

    3 days ago

    Boulder, Colorado, United States GEO Corrections & Detentions Full time

    Job SummaryWe are seeking a Quality Assurance Specialist to join our team at GEO Corrections & Detentions. As a Quality Assurance Specialist, you will be responsible for ensuring that our suppliers deliver quality parts and materials.Key ResponsibilitiesCoordinate and lead supplier development systems for new supplier evaluation, auditing, and...

  • Supplier Quality Engineer II

    4 days ago

    Boulder, Colorado, United States Medtronic Full time

    About the RoleWe are seeking a highly skilled Supplier Quality Engineer II to join our team at Medtronic. As a key member of our quality assurance team, you will be responsible for ensuring that our suppliers deliver high-quality parts, materials, and services.Key Responsibilities* Ensure that suppliers meet our quality standards and regulatory requirements*...

  • Senior Supplier Quality Engineer

    2 weeks ago

    Boulder, Colorado, United States Emerson Full time

    About the RoleWe are seeking a highly skilled Senior Supplier Quality Engineer to join our team in Boulder, Colorado. As a key member of our quality assurance team, you will play a critical role in ensuring the quality of our electrical products and services.Key ResponsibilitiesCollaborate with design engineers and suppliers to ensure that our technical and...

  • Quality Assurance Specialist

    1 week ago

    Boulder, Colorado, United States FIRST RF Full time

    Job SummaryWe are seeking a highly skilled Quality Assurance Specialist to join our team at FIRST RF. As a Quality Assurance Specialist, you will be responsible for ensuring the quality of our RF systems and ensuring compliance with industry standards.Key Responsibilities* Conduct internal audits and support AS9100 audits and customer surveys* Conduct...

  • Quality Assurance Specialist

    4 days ago

    Boulder, Colorado, United States GEO Corrections & Detentions Full time

    Job DescriptionBenefits InformationThis role is responsible for ensuring that suppliers deliver quality parts and materials to the company.Key Responsibilities:Coordinate and lead supplier development systems for new supplier evaluation, auditing, assessment, recognition, and continuous improvement roadmaps.Maintain an approved supplier list and...

  • Quality Assurance Specialist

    5 days ago

    Boulder, Colorado, United States FIRST RF Full time

    Job DescriptionAs a Quality Assurance Specialist at FIRST RF, you will play a critical role in ensuring the highest quality standards are met in the engineering and manufacturing of advanced technologies, specifically in antennas and radio frequency (RF) systems.Key Responsibilities:Conduct internal audits and support AS9100 audits and customer surveys to...

  • Senior Quality Assurance Specialist

    4 days ago

    Boulder, Colorado, United States Blue Canyon Technologies Full time

    Job SummaryWe are seeking a highly skilled Senior Quality Assurance Specialist to join our team at Blue Canyon Technologies. As a key member of our quality assurance team, you will be responsible for ensuring that our products meet the highest standards of quality and reliability.The ideal candidate will have a strong background in electrical inspection and...

  • Quality Assurance Manager

    2 weeks ago

    Boulder, Colorado, United States CPS Full time

    Quality Assurance ManagerCPS is seeking a Quality Assurance Manager to oversee daily production floor activities related to quality. This individual will be responsible for supervising QA technicians, providing guidance on quality and food safety issues, and coaching the QA team to support business growth.Key Responsibilities:Supervise daily activities of QA...

  • Quality Assurance Manager

    1 week ago

    Boulder, Colorado, United States CPS Full time

    Quality Assurance ManagerAt CPS, we are seeking a Quality Assurance Manager to oversee the supervision of all daily production floor activities as it relates to quality. This individual will be responsible for coordinating quality activities and providing leadership to ensure an effective food safety and quality management system is maintained. The Quality...

  • Hardware Quality Assurance Specialist

    1 month ago

    Boulder, Colorado, United States Blue Canyon Technologies Full time

    Job SummaryBlue Canyon Technologies is seeking a highly skilled Hardware Quality Engineer II to join our team. As a key member of our quality assurance team, you will be responsible for providing support and data to various process owners to facilitate continuous improvement initiatives, interfacing with technical engineering disciplines and manufacturing...

  • Quality Assurance Specialist

    1 month ago

    Boulder, Colorado, United States Blue Canyon Technologies Full time

    Job DescriptionBlue Canyon Technologies, a leading manufacturer of small satellites, is seeking a Quality Inspector II to join their team. As a Quality Inspector II, you will play a critical role in ensuring that our products meet engineering and customer requirements.Key Responsibilities:Inspect mechanical hardware using calipers, micrometers, height gages,...

  • Quality Assurance Specialist

    4 days ago

    Boulder, Colorado, United States Medtronic Full time

    Job DescriptionAt Medtronic, we are committed to improving human welfare by advancing healthcare, society, and equity through innovative technologies. We are seeking a highly skilled Quality Assurance Specialist to join our team.The successful candidate will be responsible for developing and maintaining quality assurance programs to ensure compliance with...

  • Quality Assurance Specialist

    3 weeks ago

    Boulder, Colorado, United States FIRST RF CORPORATION Full time

    Job SummaryWe are seeking a highly skilled Quality Inspector to join our team at FIRST RF CORPORATION. As a Quality Inspector, you will be responsible for ensuring the quality of our products, including antennas and radio frequency (RF) systems.Key Responsibilities:Conduct visual inspections of products to ensure they meet quality standardsPerform...

  • Quality Assurance Specialist II

    4 days ago

    Boulder, Colorado, United States Blue Canyon Technologies Full time

    Job OverviewBlue Canyon Technologies is seeking a Quality Inspector II to ensure the quality of our spaceflight components. As a key member of our team, you will be responsible for inspecting and verifying the quality of our products, including circuit boards, mechanical hardware, and other subassembly components.Key Responsibilities:Inspect and verify the...

  • Quality Assurance Specialist

    4 weeks ago

    Boulder, Colorado, United States KBR Full time

    Job Title: Quality Assurance SpecialistKBR is seeking a Quality Assurance Specialist to perform surveillance activities and hardware quality assurance functions on space instruments, components, subsystems, and subassemblies with contract, KBR, and requirements.Responsibilities:Support the development and implementation of mission assurance requirements over...

  • Quality Assurance Specialist

    2 weeks ago

    Boulder, Colorado, United States KBR Full time

    Job Title: Quality Assurance SpecialistKBR is seeking a Quality Assurance Specialist to perform surveillance activities and hardware quality assurance functions on space instruments, components, subsystems, and subassemblies. The successful candidate will be responsible for ensuring compliance to contract, KBR, and requirements.Responsibilities:Support the...

  • Quality Assurance Specialist, IVD

    1 month ago

    Boulder, Colorado, United States Danaher Corporation Full time

    Job SummaryAt Danaher Corporation, we are seeking a highly skilled Quality Systems Specialist, IVD to join our team. As a key member of our Quality Assurance and Regulatory Affairs Department, you will play a critical role in ensuring the quality and compliance of our products.Key ResponsibilitiesMaintain accurate and up-to-date records and processes for...

  • Quality Assurance Specialist

    1 month ago

    Boulder, Colorado, United States KBR Full time

    Job Title: Quality Assurance SpecialistKBR is seeking a Quality Assurance Specialist to perform surveillance activities and hardware quality assurance functions on space instruments, components, subsystems, and subassemblies with contract, KBR, and requirements.Responsibilities:Support the development and implementation of mission assurance requirements over...

  • Quality Assurance Specialist, IVD

    4 weeks ago

    Boulder, Colorado, United States Danaher Corporation Full time

    About the RoleWe are seeking a highly skilled Quality Systems Specialist to join our team at Danaher Corporation. As a key member of our Quality Assurance and Regulatory Affairs Department, you will play a critical role in ensuring the quality and compliance of our products.Key ResponsibilitiesMaintain accurate and up-to-date records and processes for...