26 days old

QA Associate-Validation

Aesculap Biologics
Breinigsville, PA 18031
  • Job Code
    117355423
Aesculap Biologics


QA Associate-Validation

US-PA-Breinigsville

Job ID: 2020-15822
Type: Regular Full-Time
# of Openings: 1
Category: Quality
Aesculap Biologics LLC

Overview

Aesculap Biologics, LLC, was established in January 2012 as a division of Aesculap, Inc. and is focused on biological approaches to the repair and regeneration of diseased or damaged tissues. Using a combination of cells, growth factors and smart biomaterial devices, Aesculap Biologics products can stimulate and support the synthesis of new tissue and enhance the body’s own regenerative power to improve the quality of patient’s lives.



Responsibilities

Position Summary:

The position will be responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for equipment, systems, and processes in support of Cell therapy manufacturing operations to assure compliance with cGMPs and Good Tissue Practices. This position will work with stakeholders to maintain the GMP status of equipment, systems, and processes. The QA Associate-Validation is responsible for project management to set and meet lead times to ensure validation, periodic assessment and requalification projects stay on schedule. This position is also responsible for product safety and quality and has a direct impact on patient safety. All job functions must be carried out responsibly, competently and conscientiously to ensure that Aesculap Biologics’ products are safe and effective.

Responsibilities: Essential Duties

  • Interprets and understands relevant laws and standards and provides guidance to Operations, Development and Quality staff to provide instruction, advice, and enforcement of GMP/GTP compliance.
  • Reviews, and approves SOPs, validations, quality system records, and other documents for accuracy, consistency and compliance with relevant federal and state regulations.
  • Develops/Authors technical documents including Quality system records, SOPs, work instructions, validations (URS, DDS, IOQ, PQ, UAT, Reports), investigations, etc. in compliance to applicable laws and standards.
  • Executes and manages periodic assessment and requalifications for controlled temperature units (CTUs), lab instruments, computerized systems, processes, and facilities.
  • Conducts thermal validation testing using thermocouple sensors and data collection instruments (Kaye Valprobe, AVS) on equipment including GMP controlled temperature units (CTUs).
  • Executes and manages risk assessment, planning, and execution/mitigation activities to ensure the quality of equipment, systems, processes used in the manufacture of product are maintained throughout their lifecycles.
  • Manages suppliers/contractors contracted to perform GxP functions (installation, commissioning, validation), as required.
  • Manages the Site Validation Master Plan.
  • Performs technical reviews and interprets data for accuracy of equipment/process performance for completed validations/revalidations
  • Conducts system administration activities for computerized systems (e.g. user management, periodic maintenance, updates, etc.), as required.
  • Maintains metrics for periodic assessment/requalification activities.
  • Participates in cross-functional design, development, improvement and investigative activities (root cause analysis). Capable of applying a use of Quality Tools, such as FMEA, in design, development, improvement and investigative activities.
  • Performs internal and external audits to GMP/GTP compliance, Quality Standards, and Aesculap Biologics’ policies and procedures.
  • Prepares audit plans and reports and develops corrective and preventive action and subsequent follow up activities to ensure corrections.
  • Facilitates and actively participates in third party and regulatory inspection activities (PAI).
  • Creates, prepares, and presents Quality System Management Review and GMP training.
  • Must comply with applicable ISO and FDA regulations as stated in Quality Manual
  • Must embody the Company’s Vision, Mission and Values
  • Other quality related duties may be assigned at the discretion of management.
  • This position may be exposed to potentially contaminated instruments and blood or other bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, AB will provide a safe working environment for all employees.
  • The ability to gown and mask for performance or observation of aseptic processing in a clean room environment is required.

Expertise: Knowledge & Skills

  • Language Skills: Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to top management, public groups, and/or boards of directors.
  • Mathematical Skills: Ability to add, subtract, multiply, divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
  • Reasoning Ability: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.


Qualifications

Expertise: Qualifications - Experience/Training/Education/Etc

Required:

  • BS/BA degree in the life sciences, engineering, or related field is required.
  • 0-3 years of Quality System / GMP experience in Pharmaceutical, Biotech or Medical Device industry is desirable.
  • The ability to process, analyze, and present data for the effective presentation of concepts and ideas. Some knowledge of basic statistical analysis is required.
  • Must have ability to exercise judgement and prioritize and execute the appropriate course of action(s) as dictated by the complexity of the scenario.
  • Must be adaptable, customer service oriented, have a positive attitude.
  • Must be detail oriented and have strong organizational skills.
  • Must be able to work independently and effectively as part of a team, exhibiting effective interpersonal skills.
  • Strong Computer skills in spreadsheet and word processing applications is required.
  • Excellent technical oral and written communication skills are required.
  • Working knowledge and experience with process improvement and analysis tools (e.g. Pareto analysis, control charts, Root Cause analysis, FMEA, etc.) is a plus.
  • The ability to interpret the cGMPs/GTPs, federal and state regulatory requirements is a plus.
  • Experience with Document Management, Training Management, Maintenance Management and ERP systems is a plus.

Secondary or peripheral job functions: N/A

Supervisory Responsibilities: N/A

While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds.

B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com.

Through its “Sharing Expertise®” initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.



All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

PI117355423

<b>Aesculap Biologics</b><br/><br/><br/><b>QA Associate-Validation</b><br/><br/>US-PA-Breinigsville<br/><br/><b>Job ID:</b> 2020-15822<br/><b>Type:</b> Regular Full-Time<br/><b># of Openings:</b> 1<br/><b>Category:</b> Quality<br/>Aesculap Biologics LLC<br/><br/><b>Overview</b><br/><br/><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif; color: black;">Aesculap Biologics, LLC, was established in January 2012 as a division of Aesculap, Inc. and is focused on biological approaches to the repair and regeneration of diseased or damaged tissues. Using a combination of cells, growth factors and smart biomaterial devices, Aesculap Biologics products can stimulate and support the synthesis of new tissue and enhance the bodys own regenerative power to improve the quality of patients lives. </span></p><br/><br/><b>Responsibilities</b><br/><br/><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"><strong>Position Summary:</strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;">The position will be responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for equipment, systems, and processes in support of Cell therapy manufacturing operations to assure compliance with cGMPs and Good Tissue Practices. This position will work with stakeholders to maintain the GMP status of equipment, systems, and processes. The QA Associate-Validation is responsible for project management to set and meet lead times to ensure validation, periodic assessment and requalification projects stay on schedule. This position is also responsible for product safety and quality and has a direct impact on patient safety. All job functions must be carried out responsibly, competently and conscientiously to ensure that Aesculap Biologics products are safe and effective. </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"> <strong>Responsibilities: Essential Duties</strong></span></p><p style="margin: 0px;"> </p><ul><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Interprets and understands relevant laws and standards and provides guidance to Operations, Development and Quality staff to provide instruction, advice, and enforcement of GMP/GTP compliance. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Reviews, and approves SOPs, validations, quality system records, and other documents for accuracy, consistency and compliance with relevant federal and state regulations.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Develops/Authors technical documents including Quality system records, SOPs, work instructions, validations (URS, DDS, IOQ, PQ, UAT, Reports), investigations, etc. in compliance to applicable laws and standards.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Executes and manages periodic assessment and requalifications for controlled temperature units (CTUs), lab instruments, computerized systems, processes, and facilities. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Conducts thermal validation testing using thermocouple sensors and data collection instruments (Kaye Valprobe, AVS) on equipment including GMP controlled temperature units (CTUs).</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Executes and manages risk assessment, planning, and execution/mitigation activities to ensure the quality of equipment, systems, processes used in the manufacture of product are maintained throughout their lifecycles. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Manages suppliers/contractors contracted to perform GxP functions (installation, commissioning, validation), as required. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Manages the Site Validation Master Plan.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Performs technical reviews and interprets data for accuracy of equipment/process performance for completed validations/revalidations</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Conducts system administration activities for computerized systems (e.g. user management, periodic maintenance, updates, etc.), as required. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Maintains metrics for periodic assessment/requalification activities. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Participates in cross-functional design, development, improvement and investigative activities (root cause analysis). Capable of applying a use of Quality Tools, such as FMEA, in design, development, improvement and investigative activities. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Performs internal and external audits to GMP/GTP compliance, Quality Standards, and Aesculap Biologics policies and procedures. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Prepares audit plans and reports and develops corrective and preventive action and subsequent follow up activities to ensure corrections. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Facilitates and actively participates in third party and regulatory inspection activities (PAI).</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Creates, prepares, and presents Quality System Management Review and GMP training. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must comply with applicable ISO and FDA regulations as stated in Quality Manual</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must embody the Companys Vision, Mission and Values</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Other quality related duties may be assigned at the discretion of management. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">This position may be exposed to potentially contaminated instruments and blood or other bodily fluids. In compliance with Occupational Safety and Health Administration (OSHA) regulations, AB will provide a safe working environment for all employees. </span></li><li><span style="font-size: 12pt; font-family: calibri, sans-serif;">The ability to gown and mask for performance or observation of aseptic processing in a clean room environment is required.</span></li></ul><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"><strong>Expertise: Knowledge & Skills</strong></span></p><ul><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Language Skills: Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to effectively present information to top management, public groups, and/or boards of directors. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Mathematical Skills: Ability to add, subtract, multiply, divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Reasoning Ability: Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables. </span></li></ul><br/><br/><b>Qualifications</b><br/><br/><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"><strong>Expertise: Qualifications - Experience/Training/Education/Etc</strong></span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"><strong>Required:</strong></span></p><ul><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">BS/BA degree in the life sciences, engineering, or related field is required.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">0-3 years of Quality System / GMP experience in Pharmaceutical, Biotech or Medical Device industry is desirable. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">The ability to process, analyze, and present data for the effective presentation of concepts and ideas. Some knowledge of basic statistical analysis is required. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must have ability to exercise judgement and prioritize and execute the appropriate course of action(s) as dictated by the complexity of the scenario. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must be adaptable, customer service oriented, have a positive attitude.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must be detail oriented and have strong organizational skills.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Must be able to work independently and effectively as part of a team, exhibiting effective interpersonal skills. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Strong Computer skills in spreadsheet and word processing applications is required. </span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Excellent technical oral and written communication skills are required.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">Working knowledge and experience with process improvement and analysis tools (e.g. Pareto analysis, control charts, Root Cause analysis, FMEA, etc.) is a plus.</span></li><li><span style="font-family: calibri, sans-serif; font-size: 12pt;">The ability to interpret the cGMPs/GTPs, federal and state regulatory requirements is a plus.</span></li><li><span style="font-size: 12pt; font-family: calibri, sans-serif;">Experience with Document Management, Training Management, Maintenance Management and ERP systems is a plus.</span></li></ul><p style="margin-right: -1.1pt;"><span style="font-family: calibri, sans-serif; font-size: 12pt;">Secondary or peripheral job functions: N/A</span></p><p style="margin-right: -1.1pt;"><span style="font-family: calibri, sans-serif; font-size: 12pt;"> </span></p><p style="margin-right: -1.1pt;"><span style="font-family: calibri, sans-serif; font-size: 12pt;">Supervisory Responsibilities: N/A </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;">While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to use hands to handle or feel and reach with hands and arms. The employee is occasionally required to stand and walk. The employee must occasionally lift and/or move up to 20 pounds.</span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;">B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement. To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com.</span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: calibri, sans-serif;">Through its Sharing Expertise initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.</span></p><br/><br/>All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. <img src="https://analytics.click2apply.net/v/eo2q7ecNQ1KNijxYhmLOY"> <p>PI117355423</p>

Categories

Posted: 2020-01-23 Expires: 2020-02-23

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

QA Associate-Validation

Aesculap Biologics
Breinigsville, PA 18031

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast