CQV Engineer

2 months ago

Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time
Roles & Responsibilities

PharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world with their cost-effective and high-standard healthcare products. At PharmEng Technology, we strive to cultivate the best working environment where empowerment, passion and perseverance are nurtured while serving our clients to achieve their unique business goals. We are seeking an experienced Commissioning / Qualification and Verification (CQV) Engineer with solid experience in pharmaceutical engineering, equipment qualification and pharmaceutical solutions in the Life Science industries for a role in Singapore.


Objectives of this Role:

As a CQV Engineer, you will be responsible for the executing of Commissioning and Qualification tasks within a variety of small to large scale projects. You will manage CQV projects individually as well as work within a multi-disciplinary team where you can have great influence and responsibilities. This role requires a full-time commitment with on-site presence at our client's office in Singapore.


You will ensure that the validated status of site facilities, utilities, equipment and processes is established and maintained in accordance with internal procedures, regulatory requirements and industry guidance/standards and provide expertise for the investigation and compliant resolution of non-conformances encountered during (re)qualification/(re)validation activities and site unplanned events.


Your assignments will vary from conceptual or basic design of new laboratories or manufacturing facilities to consultancy and advice on maintenance management and improvement of maintenance planning as well as technical audits. All work undertaken needs to be in accordance with the agreed budget, timescale, quality and performance criteria within the required procedures (health and safety, GMP, local and corporate standards). With your extended experience in CQV engineering and preferably project management you would be considered a great and valuable asset to our company.


The CQV Engineer will develop CQV planning documents to manage CQV projects and generate and execute CQV protocols using Good Documentation Practices (GDPs). He will investigate and resolve protocol exceptions or discrepancies and develop technical reports and CQV summary reports. He also reads and verifies facility and equipment drawings (e.g., P&IDs, ), develops Standard Operating Procedures (SOPs), process workflows, Validation Master Plans, User Requirement Specifications, Turnover Packages, and other regulatory support documentation and performs risk assessments and impact assessments.


Skills and Qualifications:

• Bachelor’s or Master’s degree in Mechanical Engineering, Chemical Engineering, Science or related technical field;

• Solid engineering (5-7 years) experience with specific experience within (bio) pharmaceutical (or related industries) and GMP is desirable; junior with a minimum of 2 years is welcome to apply.

• Proven experience in projects coordination, engineering and CQV for bio process equipment and process support systems.

• Willing to take initiative, being proactive, taking responsibility and ownership;

• Strong communicative and interpersonal skillset;

• Customer-oriented, passionate and able to effectively switch between different assignments;

• Ambitious and enthusiastic relation builder with a quality-driven mindset;

• Proficient in English, both in speaking and in writing.


Why PharmEng Technology?

Our consultants come from different areas of the Pharmaceutical/Biotech/Medical Device industries and have extensive experiences obtained from world-class organizations in North America, Europe, and Asia. At PharmEng Technology, we value everyone’s unique talents and work together to support our clients. We offer continuous career growth, competitive wages, opportunities for travel and a team mentality that sets us apart from our competitors. It is the growth of our staff that continues to grow our company globally.


EEOC Statement

At PharmEng Technology, we don’t just accept difference — we celebrate it, we support it, and we thrive on it for the benefit of our employees, our clients, and our community. PharmEng Technology is proud to be an equal opportunity workplace.


Tell employers what skills you have

Maintenance Management
cGMP Manufacturing
Regulatory Affairs
Healthcare
cGMP Practices
GMP
Investigation
Technical Audits
Protocol
Equipment Qualification
Writing
Regulatory Requirements
Pharmaceuticals
Manufacturing
Chemical Engineering
Turnover
Commissioning
Mechanical Engineering

  • Cqv / Validation Engineer

    2 weeks ago

    Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full time

    Position: CQV Engineer in SingaporeJob Description:We are currently expanding our team and are looking for a CQV Engineer for our project on site with our client.You will be responsible for planning, writing, implementing and reviewing Validation protocols in place within highly regulated environments. Your expertise will lend a hand in tactical...

  • Cqv Project Manager

    2 weeks ago

    Singapore PES International Full time

    Senior CQV Project ManagerBiotechnology ManufacturingCompany: PES InternationalLocation: Portsmouth, New HampshireCompensation: Commensurate with ExperienceAbout this opportunity:PES International is an international industry leader in providing automation, commissioning, qualification, and CSV services. We have an unrivaled knowledge based in these...

  • Senior Cqv Engineer

    2 weeks ago

    Singapore PES International Full time

    PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational...

  • QA Validation Engineer- Cqv/csv

    2 weeks ago

    Singapore PROCESS ENGINEERING SPECIALISTS PTE. LTD. Full time

    PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational clients.We...

  • Senior Csv Engineer

    2 weeks ago

    Singapore PM Group Full time

    Senior CSV Engineer: Contract Onsite Singapore, Singapore CQV 731 SGD**Overview We have an immediate requirement for 2- CSV Specialists to join a highly skilled PM Group team based on a client site.**ResponsibilitiesDay to day activities include the following_:_**- Commissioning and Qualification of hardware and associated software to support Utility/Process...

  • Senior Validation/Validation Engineer

    4 weeks ago

    Singapore ESCO ASTER PTE. LTD. Full time

    Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

  • Senior Validation/Validation Engineer

    4 weeks ago

    Singapore ESCO ASTER PTE. LTD. Full time

    Roles & ResponsibilitiesThe OpportunityEsco Lifesciences Group, is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 20 countries across North America, Europe and Asia.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first introduced in 2017.At Esco Aster Pte Ltd, we...

  • Junior Validation Engineers-gmp/pharma

    2 weeks ago

    Singapore PES International Full time

    PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes for our multinational...

  • Senior Validation Engineer

    2 weeks ago

    Singapore No deviation Pte Ltd Full time

    Responsibilities: Responsible for planning, executing and closing out the validation activities within the assigned area. Develop required validation documents, including Risk Assessments, plans, protocols, and reports. Review, analyse, interpret and summarise data of executed studies. Investigate or support the investigating of deviations or nonconformities...

  • Senior Validation Engineer

    2 weeks ago

    Singapore No Deviation Pte Ltd Full time

    No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We strongly uphold our core...

  • Cqv Engineer(Change Controls Owner)

    2 weeks ago

    Singapore PROCESS ENGINEERING SPECIALISTS PTE. LTD. Full time

    PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational...

  • HVAC Qualification Engineer

    1 month ago

    Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full time

    Roles & ResponsibilitiesWe are Coalesce Management Consulting! A community of people with strong Passion for ExcellenceWe deliver bespoke project solutions within Life Science and Technology sectors by Consultative through our community of High Calibre Industry specialists.Our approach is Simple but meaningful – We Grow by Helping Others Grow, We pride...

  • Junior Master Data

    2 weeks ago

    Singapore No deviation Pte Ltd Full time

    About NdIncorporated in 2007, we are a patient-centric solution provider for the pharmaceutical industry. We are experts in engineering consultancy, commissioning, qualification and validation services, and regulatory quality/compliance in Asia and Europe.We offer personalized focused solutions for the pharmaceutical industry in engineering consultancy and...

  • Consultant SAP Pm Application

    2 weeks ago

    Singapore No deviation Pte Ltd Full time

    Overview:Who We Are: No Deviation is a provider of patientcentric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services. We...

  • Commissioning and Qualification Specialist

    3 months ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesResponsibilities: Provide direct services to site Technical Services management, contributing to increased throughput of commissioning and qualification activities across the site. Collaborate with Technical Services management while independently performing required validation activities. Support C&Q activities across the site as...

  • Commissioning and Qualification Specialist

    4 weeks ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesResponsibilities: Provide direct services to site Technical Services management, contributing to increased throughput of commissioning and qualification activities across the site. Collaborate with Technical Services management while independently performing required validation activities. Support C&Q activities across the site as...

  • Validation Consultant

    2 weeks ago

    Singapore Triton AI Pte Ltd Full time

    Perform risk-based commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following areas:Process Equipment CIP / SIP Process Manufacturing and related business processes including Quality Operations and Supply Chain Operations Method validation (analytical chemistry, biochemistry,...

  • Quality Assurance Specialist

    2 weeks ago

    Singapore No deviation Pte Ltd Full time

    No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We strongly uphold our core...

  • Validation Consultant

    2 weeks ago

    Singapore TRITON AI PTE. LTD. Full time

    Up to $7000 with 2 months Variable Bonus, Permanent Position:- West Singapore:- Pharmaceutical Industry Experience is a MUST:Experiences in multiple CQV discipline (such as CIP, SIP)Responsibilities: Perform riskbased commissioning, qualification and validation service for pharmaceutical and biopharmaceutical clients on one or more of the following...

  • Office Administrator

    2 weeks ago

    Singapore No deviation Pte Ltd Full time

    No Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We strongly uphold our core...