Cqv Engineer

Job Description About PSC Biotech   Who we are?
  PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide.
We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.
  'Take your Career to a new Level'   PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry.
We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.
  Employee Value Proposition   Employees are the "heartbeat" of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression.
We believe in creating high performing teams that can exceed our client's expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Job Title: CQV Engineer.
Role Description: As part of a significant expansion of the client site, an exciting opportunity has come to join the science, engineering/ manufacturing & commercialisation team to support the high potency facility from construction, project phase to a fully operational facility delivering life-saving products to patients.
  The Area: There are 4 broad technical areas that will require the leadership of experienced, energetic and committed engineers – ·         Sterilisation & Temperature Mapping – Autoclaves & CTUs ·         Cleaning – Parts Washer ·         Vial and Syringe (and cartridge) filling operations – Glass handling, Tray & Tub handling, Drug Product Filling and Parenteral Product Visual Inspection.
·         Vial and Syringe Sterility operations – Isolators, VHP ·         Fill Finish ancillary equipment – FIT, GIT, Tube Welders/ Sealers ·         The successful candidate will need to have demonstrated in-depth experience in 3 or more of these areas.
Requirements Role Functions: The successful candidate will be involved in the project from Detailed Design, Construction, Site Acceptance Test (SAT) at the earliest, responsible for C&Q deliverables and follow assigned systems through to through to the Equipment Performance Qualification, Validation and Product PQ – including filing with regulatory bodies.
Each role will be involved in the project from the vendor Factory Acceptance Test (FAT), at the earliest, through to the Performance Qualification.
   Levels of responsibility will vary during this timeframe as outlined below – ·         Factory Acceptance Test – Attendance, hands-on support and C&Q Oversight ·         Installation to Mechanically Complete – C&Q Oversight ·         Commissioning & Qualification – Hands-on support & Oversight throughout project lifecycle ·         Cycle Development – Execution of Cycle Development pre and post OQ phases ·         Performance Qualification – Responsibility for / Execution of all Performance Qualification testing.
  The Expectations: Within your chosen role you will be acting as an intermediate engineer reporting within the GSEC model to Technical Engineering department, the role will include - ·         Engage in the early stages of the project, giving input into design by working with equipment vendors and global engineering teams, attending FAT and design reviews to represent client validation interests.
Oversee equipment C&Q within the assigned area with a view to ensuring right first-time C&Q and Validation effort.
·         Act as C&Q SME on the equipment within the area assigned.
  ·         As such you will be executing with a view to leveraging testing from Commissioning and Qualification to PQ where possible.
·         Providing technical and validation oversight to process, design and project delivery teams and coaching to associate staff within the assigned suite.
·         Implementing the requirements as outlined in the site / C&Q and project Validation Master Plan.
·         Coordination of engineering sub-teams in the assigned suite during execution of IQ/OQ / Cycle Development & Validation activities.
·         Authoring and reviewing standard operating procedures and technical reports including IOC/ IOQ & PQ protocols.
·         Technical owner of Commissioning protocols, Qualification protocols and input to Validation protocols executed by vendors, cross functional groups and/ or validation counterparts.
·         Supporting regulatory submissions as required.
·         Input to Change Management process for Equipment introduction within the assigned suite for qualification / validation up to PQ stage.
·         Effective application of Lean Six Sigma and Change Management tools in the Validation group by: ·         Leading by example in achieving results by using industry standard tools and processes ·         Facilitate problem solving & risk assessment (FMEA) projects/meeting.
·         Make problems visible and strive for continuous improvement.
·         Serving as a key member during internal audits and external inspections/audits.
·         Support various organizational initiatives as needed (examples include EHS, workload forecasting, work standardization, etc).
·         Keep up to date with scientific and technical developments, best practices and attend seminars as required.
·         Maintain continuous focus on quality and safety compliance and unflinching focus on the customer.
  Experience, Knowledge & Skills: Preferred Experience and Skills: ·         This role requires an experienced individual with a minimum of 3 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
·         A self-starter and results-focussed, the successful candidate will have strong contemporary knowledge, and the ability to work independently and on multidisciplinary teams.
·         The successful candidate will also have demonstrated the ability to deliver what is needed on-time, holding self and team members accountable for commitments, decisions, actions and behaviours.
·         S/he will also have excellent oral and written communication skills, with the ability to effectively articulate understanding of process science, in order to drive decision making, impact assessments, design of studies, etc., in a multi-disciplinary team environment.
·         With relevant technical qualification(s) in Applied Pharmaceutical / Biological / Computer / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
·         The candidate will also show ambition and drive to develop and advance within the role.
  Preferred Experience and Skills: ·         Minimum 3 years process equipment C&Q/ Validation experience on Large Scale Projects ·         SME on Equipment Validation on any of; Parts Washer / Autoclaves / Vaporised Hydrogen Peroxide Sterilising Isolators / Clean Utilities - Transfer Panels & Formulation / Visual Inspection/ Single Use Technologies ·         Working knowledge of ASTM E2500 / Eudralex / FDA / ISPE guidelines / Revised Annex 1 ·         Experience with liaising with other departments – engineering, technical, operations and QA ·         Experience with sterile processing and sterilisation technologies ·         Experience with cleaning and process validation, technology transfer, regulatory filing, and commercial drug product manufacturing of biologics is a plus.
·         Prior experience in drug product processing equipment, PQ, Process Performance Qualification and Validation, site readiness, batch record reviews, authoring documents subject to regulatory inspection.
·         Autoclave Qualification and Sterilisation Loads Cycle Development experience ·         Use of temperature mapping equipment such as Lives/ Kaye etc.
and trending, analysing and interpreting complex data   Desirable but not essential: ·         Visual Inspection technologies for Vial & Syringe ·         Vial & Syringe processing technologies; drug product filling, glass handling, tray handling, stoppering, capping and CCI.
·         Formulation and Clean Utilities C&Q along with Single Use Technologies ·         Warehouse and CTU qualification advantageous ·         New facility brown/ green field facility experience ·         Small equipment qualification and validation; FITs, Scales, Tube Sealers/ Welders, Headspace analysers, Flowmeters, Mobile Vessels & Single Use Technologies.
·         Project Management experience / training in use of Project Management tools.
  Qualifications & Education: ·         This role requires an experienced individual with a minimum of 3 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
Applicants with less than 3 years of direct experience may be considered for future, more junior roles.
·         A self-starter and results-focussed, the successful candidate will have strong contemporary knowledge, and the ability to work independently and on multidisciplinary teams.
·         The successful candidate will also have demonstrated the ability to deliver what is needed on-time, holding self and team members accountable for commitments, decisions, actions, and behaviours.
·         S/he will also have excellent oral and written communication skills, with the ability to effectively articulate understanding of process science, to drive decision making, impact assessments, design of studies, etc., in a multi-disciplinary team environment.
·         With relevant technical qualification(s) in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
·         The candidate will also show ambition and drive to develop and advance within the role.
#LI-BR1 Requirements Role Functions: The successful candidate will be involved in the project from Detailed Design, Construction, Site Acceptance Test (SAT) at the earliest, responsible for C&Q deliverables and follow assigned systems through to through to the Equipment Performance Qualification, Validation and Product PQ – including filing with regulatory bodies.
Each role will be involved in the project from the vendor Factory Acceptance Test (FAT), at the earliest, through to the Performance Qualification.
Levels of responsibility will vary during this timeframe as outlined below – · Factory Acceptance Test – Attendance, hands-on support and C&Q Oversight · Installation to Mechanically Complete – C&Q Oversight · Commissioning & Qualification – Hands-on support & Oversight throughout project lifecycle · Cycle Development – Execution of Cycle Development pre and post OQ phases · Performance Qualification – Responsibility for / Execution of all Performance Qualification testing.
The Expectations: Within your chosen role you will be acting as an intermediate engineer reporting within the GSEC model to Technical Engineering department, the role will include - · Engage in the early stages of the project, giving input into design by working with equipment vendors and global engineering teams, attending FAT and design reviews to represent client validation interests.
Oversee equipment C&Q within the assigned area with a view to ensuring right first-time C&Q and Validation effort.
· Act as C&Q SME on the equipment within the area assigned.
· As such you will be executing with a view to leveraging testing from Commissioning and Qualification to PQ where possible.
· Providing technical and validation oversight to process, design and project delivery teams and coaching to associate staff within the assigned suite.
· Implementing the requirements as outlined in the site / C&Q and project Validation Master Plan.
· Coordination of engineering sub-teams in the assigned suite during execution of IQ/OQ / Cycle Development & Validation activities.
· Authoring and reviewing standard operating procedures and technical reports including IOC/ IOQ & PQ protocols.
· Technical owner of Commissioning protocols, Qualification protocols and input to Validation protocols executed by vendors, cross functional groups and/ or validation counterparts.
· Supporting regulatory submissions as required.
· Input to Change Management process for Equipment introduction within the assigned suite for qualification / validation up to PQ stage.
· Effective application of Lean Six Sigma and Change Management tools in the Validation group by: · Leading by example in achieving results by using industry standard tools and processes · Facilitate problem solving & risk assessment (FMEA) projects/meeting.
· Make problems visible and strive for continuous improvement.
· Serving as a key member during internal audits and external inspections/audits.
· Support various organizational initiatives as needed (examples include EHS, workload forecasting, work standardization, etc).
· Keep up to date with scientific and technical developments, best practices and attend seminars as required.
· Maintain continuous focus on quality and safety compliance and unflinching focus on the customer.
Experience, Knowledge & Skills: Preferred Experience and Skills: · This role requires an experienced individual with a minimum of 3 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
· A self-starter and results-focussed, the successful candidate will have strong contemporary knowledge, and the ability to work independently and on multidisciplinary teams.
· The successful candidate will also have demonstrated the ability to deliver what is needed on-time, holding self and team members accountable for commitments, decisions, actions and behaviours.
· S/he will also have excellent oral and written communication skills, with the ability to effectively articulate understanding of process science, in order to drive decision making, impact assessments, design of studies, etc., in a multi-disciplinary team environment.
· With relevant technical qualification(s) in Applied Pharmaceutical / Biological / Computer / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
· The candidate will also show ambition and drive to develop and advance within the role.
Preferred Experience and Skills: · Minimum 3 years process equipment C&Q/ Validation experience on Large Scale Projects · SME on Equipment Validation on any of; Parts Washer / Autoclaves / Vaporised Hydrogen Peroxide Sterilising Isolators / Clean Utilities - Transfer Panels & Formulation / Visual Inspection/ Single Use Technologies · Working knowledge of ASTM E2500 / Eudralex / FDA / ISPE guidelines / Revised Annex 1 · Experience with liaising with other departments – engineering, technical, operations and QA · Experience with sterile processing and sterilisation technologies · Experience with cleaning and process validation, technology transfer, regulatory filing, and commercial drug product manufacturing of biologics is a plus.
· Prior experience in drug product processing equipment, PQ, Process Performance Qualification and Validation, site readiness, batch record reviews, authoring documents subject to regulatory inspection.
· Autoclave Qualification and Sterilisation Loads Cycle Development experience · Use of temperature mapping equipment such as Lives/ Kaye etc.
and trending, analysing and interpreting complex data Desirable but not essential: · Visual Inspection technologies for Vial & Syringe · Vial & Syringe processing technologies; drug product filling, glass handling, tray handling, stoppering, capping and CCI.
· Formulation and Clean Utilities C&Q along with Single Use Technologies · Warehouse and CTU qualification advantageous · New facility brown/ green field facility experience · Small equipment qualification and validation; FITs, Scales, Tube Sealers/ Welders, Headspace analysers, Flowmeters, Mobile Vessels & Single Use Technologies.
· Project Management experience / training in use of Project Management tools.
Qualifications & Education: · This role requires an experienced individual with a minimum of 3 years directly related experience in academia, pharmaceutical or biotechnology industry – along with a working knowledge of current regulatory requirements and current Good Manufacturing Practices.
Applicants with less than 3 years of direct experience may be considered for future, more junior roles.
· A self-starter and results-focussed, the successful candidate will have strong contemporary knowledge, and the ability to work independently and on multidisciplinary teams.
· The successful candidate will also have demonstrated the ability to deliver what is needed on-time, holding self and team members accountable for commitments, decisions, actions, and behaviours.
· S/he will also have excellent oral and written communication skills, with the ability to effectively articulate understanding of process science, to drive decision making, impact assessments, design of studies, etc., in a multi-disciplinary team environment.
· With relevant technical qualification(s) in Applied Pharmaceutical / Biological / Chemical sciences or applied Technical / Engineering qualification, the successful candidate will also have a proven track record in delivering excellence.
· The candidate will also show ambition and drive to develop and advance within the role.
#LI-EB1