Company

Purdue Pharma L.P.See more

addressAddressWilson, NC
type Form of workFull-Time
CategoryManufacturing

Job description

Sr. Quality Specialist I, Lab Metrology
Wilson, NC, USA Req #223
Friday, September 15, 2023

Purdue Pharma L.P. and its subsidiaries develop, manufacture and market medications to meet the evolving needs of healthcare professionals, patients, and caregivers. We were founded by physicians, and we are currently led by a physician. Beyond our efforts to provide quality medications, Purdue is committed to supporting national, regional and local collaborations to drive innovations in patient care. Privately held, Purdue is pursuing a pipeline of new medications through internal research & development and strategic industry partnerships. 
For close to two decades Purdue has engaged in many initiatives to stem prescription opioid abuse. We are committed to bringing lifesaving relief to communities and individuals suffering from substance use disorder and overdose. We are currently developing or supporting the development of two essential life-saving opioid overdose reversal medications and have the capability to manufacture others for medication assisted treatment. Providing these medicines has the potential to improve and save countless lives.


We are driven by our purpose: Compassion for patients and excellence for science inspire our pursuit of new medicines. 
 

We are building an exciting path forward, and we are committed to recruiting a dedicated team of professionals who advance our expertise through a commitment to Purdue's Values: Integrity and Courage, underpinned by Innovation, and always in Collaboration with each other.

At Purdue Pharma and our subsidiaries, you have a unique career opportunity to work differently, uncover and seize new opportunities, and take a hands-on, ownership approach to your work.  We go beyond traditional roles and find creative ways to extend our skills and interests, challenging ourselves to contribute in different, meaningful ways. We strive to create an environment where you can bring your best to work each dayWe welcome the opportunity to have you on our team!

 

We respect diversity and accordingly are an equal opportunity and an affirmative action employer. Qualified applicants will receive consideration without regard to: actual or perceived race, sex or gender (including pregnancy, childbirth, lactation and related medical conditions), national origin, ancestry, citizenship status, religion, color, age, creed, sexual orientation, marital status, gender identity or gender expression (including transgender status), protected medical condition as defined by applicable state or local law, genetic information, physical or mental disability, veteran status and military service, or any other characteristic protected by local, state, or federal laws and ordinance. 


For more information about your rights under Equal Employment Opportunity, visit:

  • EEOC Know Your Rights
  • EEOC Know Your Rights (Spanish)
  • USERRA Rights
  • Family and Medical Leave Act (FMLA)
  • Employee Polygraph Protection Act (EPPA)
  • E-Verify (English and Spanish)
  • Right to Work (English and Spanish)
  • Pay Transparency Nondiscrimination Provision (English)
  • Pay Transparency Nondiscrimination Provision (Spanish)

 We strive to make our Career opportunities website accessible to all users.    If you need an accommodation to participate in the application process, please email:  careers@pharma.com.  This email is not for general employment inquiries or vendors; rather it is strictly for applicants who require assistance accessing our careers website.


Job Summary:


The Senior Quality Specialist I, Metrology will administer metrology program, maintain equipment in LIMS, provide schedules for activities, review supplied documentation, author program procedures, and ensure compliance to regulations and written procedures. Will also provide system metrics including usage, downtime, and reliability and develop a system retirement strategy and 5-year laboratory instrument requirements plan.


Primary Responsibilities:



  • Administer metrology program, maintain equipment in LIMS, provide schedules for activities, review supplied documentation, author program procedures, and ensure compliance to regulations and written procedures. Provide system metrics including usage, downtime, and reliability.

  • Manage projects involving computer system validation as it relates to laboratory systems and the data integrity of electronic data. Work in a cross-functional team on GAMP 5 validation projects to deliver laboratory instrument/software.

  • Perform Preventative maintenance and real time repair for laboratory equipment including Sotax automated systems. Ability to read schematics and perform repairs and maintenance with minimal downtime. Ability to determine validation impact of repairs and perform required change controls in TrackWise.

  • Perform maintenance, calibration, qualification, repair and troubleshooting on a variety of laboratory instruments including but not limited to HPLC, GC, TPW3, Automated Dissolution Systems, UV spectrophotometers, Balances, and pH meters and other special purpose lab equipment.

  • Provide time trending and task data; assist with departmental scheduling; manage scheduling spreadsheets to ensure that they are complete and understood and to provide detailed status reports to management.

  • Develop, author or revise, and follow strict protocols for instrument installation, operation, and performance qualification.

  • Coordinate new instrument installation, calibration and repair with technical groups and vendor; ensure appropriate documentation is in place; communicate with vendors and service personnel regarding instrumentation issues; review vendor qualification protocols and final reports for accuracy, completeness and compliance.

  • Assess current vendor calibration programs for performance, applicability and return on investment.

  • Assist with assessment of new technology and instrumentation for the labs.

  • Assist with laboratory investigations involving equipment failure, including impact assessment.

  • Train laboratory personnel or other metrology personnel in metrology activities, as appropriate.

  • Maintain the laboratory instrumentation with minimal downtime while adhering to all compliance requirements.

  • Implement new instrumentation and new technology in the laboratory including validation and qualification of systems.

  • Collaborate closely with users/laboratory colleagues to resolve issues; Assist in setting priorities for problem resolution related to the instrumentation. Assist in investigations, including root cause analysis and CAPA plan.

  • Write, revise, develop, evaluate and review Standard Operating Procedures for instrumentation.


Education and Experience:


Requires at a minimum, a BS degree in Chemistry or other related science with 8 years minimum experience or equivalent level of experience in pharmaceutical or related industries; or graduate degree (MS preferred) with 6-10 plus years experience or PhD with 3-6 plus years experience.


Necessary Knowledge, Skills and Abilities:



  • A successful history in maintaining instruments is desirable.

  • Direct experience in repair and maintenance of laboratory robotics equipment and metrology required for senior level position.

  • Must have strong oral and written communication skills.

  • The incumbent must be able to clearly identify problems or compliance issues arising from the assigned work and quickly implement solutions.

  • Candidate must have a working knowledge of USP, FDA, cGMP, GAMP (particularly V-Model) and 21 CFR Part 11 requirements.

  • Direct experience with documenting user requirements and functional specifications for laboratory instrument/automation systems preferred.

  • Knowledge of LIMS, Quality Documentation Systems, Change Control, CAPA Laboratory operations, and Stability programs is highly preferred.

  • Knowledge of HPLC, UPLC, Empower CDS, TPW3, MultiDose and other laboratory systems is required.


Supervisory Responsibilities (if applicable):


This position reports to the Senior Manager Quality Control. This person has no direct reports, however, works in a matrix environment to ensure laboratory equipment reliability, operation and compliance.


Physical and Environmental



  • Perform job functions in various positions that may require sitting, stooping, balancing, kneeling, crouching, twisting, and/or reaching. While sitting for an extended period of time on a routine basis, incumbent may use the following equipment: Personal computer, telephone/ other voice communication devices, copier, fax, scanners, or other specialized equipment used in an office setting.

  • Lift and maneuver equipment and materials weighing up to 20 pounds.

  • Take samples which may require stretching, bending, or twisting to remove product from the equipment and/or drums.

  • Use small hand and power tools to perform incidental maintenance.

  • Perform cleaning and assembly/disassembly on laboratory equipment which may require pulling, pushing, or twisting to remove equipment shields, parts and panels. Equipment and parts could weigh up to 20 pounds. Also requires operation of industrial hose (water) and physical exertion (repetitive wiping, rubbing and scrubbing) to clean equipment and laboratory surfaces.

  • Ability to work a 10 hour per day/4-day work week; 40 hours per week with overtime as required.


Additional Information
Minimum required education, experience, knowledge, skills and abilities are included in the posting. The position will be filled at the level commensurate with the successful candidate's education, experience, knowledge, skills, and abilities.


The job description is not an exhaustive list of all functions that the employee may be required to perform, and the employee may be required to perform additional functions. Additionally, the company may revise the job description at any time.


We respect diversity and accordingly are an equal opportunity and an affirmative action employer. Qualified applicants will receive consideration without regard to: actual or perceived race, sex or gender (including pregnancy, childbirth, lactation and related medical conditions), national origin, ancestry, citizenship status, religion, color, age, creed, sexual orientation, marital status, gender identity or gender expression (including transgender status), protected medical condition as defined by applicable state or local law, genetic information, physical or mental disability, veteran status and military service, or any other characteristic protected by local, state, or federal laws and ordinance. 


For more information about your rights under Equal Employment Opportunity, visit: 

  • Equal Employment Opportunity is the Law (EEO)
  • EEO is the Law Poster Supplement
  • USERRA Rights
  • Family and Medical Leave Act (FMLA)
  • Employee Polygraph Protection Act (EPPA)
  • E-Verify (English and Spanish)
  • Right to Work (English and Spanish)
  • Pay Transparency Nondiscrimination Provision (English)
  • Pay Transparency Nondiscrimination Provision (Spanish) 

We strive to make our Career opportunities website accessible to all users.    If you need an accommodation to participate in the application or hiring process, please email the Talent Acquisition team at careers@pharma.com.  This email is not for general employment inquiries or vendors; rather it is strictly for applicants who require assistance.

 

The Company does not seek or accept unsolicited resumes or CVs from recruitment agencies.  We are not responsible for any fees, commission, or any type of payment related to unsolicited resumes or CVs except as required in a written agreement between the Company and the recruitment agency or party requesting payment of a fee.

 

Under certain state law, we may be required to provide a reasonable estimate of the salary range for the jobs covered by this description.  Actual salary determinations will take into account factors such as work location, prior education or training and experience, job related knowledge, and demonstrated skills aligned with the Company's internal leveling guidelines and benchmarks. Resumes may be considered in the order they are received.

 

Beware of scams involving fraudulent job postings misrepresenting the Company. Recruitment fraud is a scam offering fictitious job opportunities. This type of fraud is normally perpetrated through fake websites, or through unsolicited e-mails claiming to be from the Company. These emails request that recipients provide personal information, and sometimes payments. To help protect yourself from fraudulent recruitment scams, we encourage you to consider the following:
  • The Company never requests money or fees for any purpose during or after the hiring process.
  • The hiring process involves at least one interview (phone, virtual or in-person). The Talent Acquisition team corresponds from email addresses with the domain "@pharma.com".
  • The Talent Acquisition team does not request or require ...
Refer code: 7056289. Purdue Pharma L.P. - The previous day - 2023-12-15 16:51

Purdue Pharma L.P.

Wilson, NC
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