Current jobs related to Quality Control Specialist - India - PSC Biotech Ltd
-
Quality Controller
3 months ago
India Jay Jay Mills Full time**Job Title **:Quality Controller** **Experience**: 1 to 3 years **Location**: India **Keyskills**: Required quality testing & strong knowledge of Textiles **Salary Range**: Salary will be offered best in the Industry
-
Global Operations Position Control
2 weeks ago
india Teamware Solutions a division of Quantum Leap Consulting Pvt. Ltd Full timeJob Title: Global Operations Position Control (GOPC) Specialist Location: Bangalore Shift Timing: 11:00 AM - 8:00 PM Position Overview: We are seeking a skilled Global Operations Position Control Specialist to join our team in Bangalore. The role involves ensuring the highest standards in controls, processes, and reporting within a dynamic global...
-
Executive - Quality Control
3 months ago
India Piramal Enterprises Full timeBusiness: PPL Digwal Department: Quality Control Location: Digwal Job Overview: To perform Quality Control actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Manager - QC Key Stakeholders: Internal: Production, QA, SCM, IT, Engineering & Maintenance, TSD & Safety External: Customers Experience: - 4-8 Year...
-
Quality Control
4 months ago
India Miracle HR Full timeGender Preference Male Number Of Vacancy 1 Industry Area Manufacturer Key Skills testing equipment, tools, or software, proficient in documentation Qualification Any Graduate Salary (Per Annum) 1.80 To 2.40 LPA Work Experience 1-3 Years Job Requirement **Requirement**: Job Location : Mumbai (Charni Road) **Responsibilities**: - Conduct inspections of raw...
-
Automotive Paint Quality Specialist
2 days ago
india Maruti Suzuki India Limited Full timeVertical : Production Engineering (PE) Department : NMQ Job Location : Manesar/Kharkhoda Job Title : AM/DM Job Role : Automotive Paint Quality Specialist Educational Qualification : BTech/BE in Paint Engineering/Production Engineering/ Chemical Engineering. Work Experience : 2 to 6 years Job Responsibilities : Automotive Paint Quality...
-
Quality Control Manager
4 months ago
india Talent Corner Full timeRoles and Responsibilities Experience: 5+Location: BhiwandiBachelor's degree in a relevant field (e.g., engineering, quality management).Strong knowledge of quality management systems, quality control tools, and industry-specific regulations. Desired Candidate Profile Perks and Benefits
-
Application Controls Specialist
2 weeks ago
India LyondellBasell Full timeBASIC FUNCTION: A Controls Specialist plays a vital role in safeguarding the organization's IT infrastructure by ensuring the effectiveness of security controls. Ensure efficiency and monitor the IT security controls (Data Validation, Authorization Controls, Data Encryption, Audit Logging and Monitoring etc) of our applications (on-prem and...
-
Quality Control Auditor
3 months ago
india Rebel Foods Full timeLocation : Chandigarh Job Description :- Daily job duties for Quality auditors vary because they travel to different business locations and work in multiple types of Audits but core responsibility is do day-to-day Quality audits. Skills and Experience: Full time course or similar experience. Proficient in Excel. Excellent Communication and analytical...
-
Quality Control Manager
4 weeks ago
India Pioneer Global Recruitment Full timeJob Summary:A Quality Control Manager in the sanitaryware industry, particularly with an engineering background, plays a vital role in ensuring that products meet specific standards of quality, safety, and functionality. Sanitaryware products like toilets, washbasins, and bidets must adhere to stringent safety, hygiene, and durability standards to endure...
-
Quality Document Controller
3 months ago
India Vectrus Full timeOverview: The Quality Document Controller (QDC) is responsible for quality checking, uploading corporate and program process documents and maintaining the support documentation to the document library known as the Vectrus Execution Model (VExM) within the Vectrus Intranet/SharePoint. The QDC will actively work with other Quality Department Team members to...
-
Retail Deputy Store Manager
1 week ago
india ScS - Sofa Carpet Specialist Full timeDepartment Retail Employment Type Full Time Location York Workplace type Onsite Compensation £, - £, / year Reporting To Store Manager What does the role involve? What qualities are we looking for? What’s in it for you? About ScS We are one of the UK’s leading sofa specialists, and you can find us on...
-
Retail Deputy Store Manager
2 days ago
india ScS - Sofa Carpet Specialist Full timeDepartment Retail Employment Type Full Time Location Darlington Workplace type Onsite Compensation £, - £, / year Reporting To Store Manager What does the role involve? What qualities are we looking for? What’s in it for you? About ScS We are one of the UK’s leading sofa specialists, and you can find us on numerous...
-
Data Quality Specialist
2 days ago
india iDeals Full timeGet to Know Us iDeals is a global B2B SaaS product company recognized as in a secure business collaboration market. Trusted by more than 1,000,000 users from 175,000 companies globally, we are on a mission to create more prosperity in the world by accelerating high-stake business decisions. We achieve this by delivering intuitive and robust software...
-
india Samvid Search Pvt Ltd Full timeRole: Assistant Manager-In Process Quality Control Qualification – Diploma / B.E. Mechatronics/ Electronics/ Mechanical Work Experience – 7~10 years Preferred Industry – Lithium – ion Battery Pack / Electrical / Electronics / White goods Function: Quality – In Process Quality Control Role Accountabilities Job Summary: The In-Process Quality...
-
Quality Assurance Specialist
4 months ago
india ResMed Full timeBrightree is a wholly owned subsidiary of ResMed (NYSE: RMD, ASX: RMD). When you work at Brightree, it’s more than just a job. You’ll be part of a team that’s driving innovation and leading the way in cloud-based patient management software. The technology allows us to provide the tools for better outcomes but at our heart, we’re really about...
-
Quality Assurance Specialist
2 days ago
india ResMed Full timeBrightree is a wholly owned subsidiary of ResMed (NYSE: RMD, ASX: RMD). When you work at Brightree, it’s more than just a job. You’ll be part of a team that’s driving innovation and leading the way in cloud-based patient management software. The technology allows us to provide the tools for better outcomes but at our heart, we’re really about...
-
Business Intelligence Developer
2 months ago
Northeast India ScS - Sofa Carpet Specialist Full timeDepartment IT Employment Type Full Time Location Sunderland - Customer Support Centre Workplace type Hybrid Reporting To BI Manager What does the role involve? Who are we looking for? What’s in it for you? About ScS We are one of the UK’s leading sofa specialists, and you can find us on numerous retail parks all over the...
-
Planning Control Specialist
2 weeks ago
india Deepak Group Co Full timeJob Summary: The ideal candidate will have a proven track record in managing large-scale projects, particularly in the oil & gas and petrochemical sectors. They will be adept at leading project control teams to achieve project objectives efficiently. Key Responsibilities: Monitor all upcoming and ongoing projects, reporting to the management team. Develop...
-
india RECON Full timeReports To: Director of Project Management / Senior Project Manager Location: New DelhiJob Type: Full-time Job OverviewWe are seeking a skilled and experienced Project Manager to oversee the construction, supervision, and quality control of residential home construction projects. The Project Manager will ensure that all aspects of the construction are...
-
Assistant Manager
2 days ago
india Unichem Laboratories Limited Full timeExperience - 10 to 16 yearsQualification - M.Sc. (Chemistry)RESPONSIBILITIESReview change controls, OOS, deviations, and other quality system investigations provided by QC / Analytical departments at the site and other locations and send the same for corporate approval.Review vendor qualification documents, including vendor questionnaires and interact with...
Quality Control Specialist
3 months ago
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 points 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.
· The purpose of this role is to work within and support the Global Development Quality Assurance team at client cite.
· This role will primarily provide support for Change Control, Deviation Management and Supplier Quality Management.
· It will also support interface of SAP with IPI Product structure and MES BOMs and recipes. Other activities to support Quality Systems and QA Operations will be required as per start up schedule.
· The QA Systems and Compliance Team with work closely with the Operations, Engineering, Validation, Supply Chain and AR&D Functions to ensure compliance to Global and Regulatory Quality Management System requirements as they pertain to the client Quality Manual, Change Control, Deviation Management, Supplier Quality Management, Quality Risk Management, Audit Management and associated electronic systems.
The role is required to:
- Participate daily on cross-functional teams to collaboratively actively to address compliance issues and achieve project milestones.
- Participate in and lead investigation of deviations, risk assessments and changes, ensuring appropriate actions are implemented timely.
- Provide QA review and approval of Change Controls, Deviations/CAPAs, SOPS and related documentation for compliance to GMP and site requirements at the facility.
- Provide QA oversight to GMP readiness, technical transfers, regulatory approvals and clinical operations at the facility.
- Assist in the development of training curricula and records for QA and providing SME training on Quality Assurance SOPs as required.
- Assist in the creation and maintenance of QA SOPs, metrics and reports in line with site requirements.
- Support an environment of continuous improvement by identifying and implementing efficiencies and quality improvements.
- Work collaboratively to foster strong relationships with management and colleagues and to drive a safe and compliant culture.
- Ensure the escalation of compliance risks to management in a timely manner.
What skills you will need:
In order to excel in this role, you will more than likely have:
- Bachelor's degree, or higher (Science/Quality/Technical).
- 4-5 years' experience, ideally in Quality Assurance, Quality Control or Technical Operations within the Biological and/or pharmaceutical industry.
- Previous experience in QRM, SQM, Deviations and Change Control, participating in investigations and problem solving.
- Strong attention to detail and precision in preparing and reviewing GMP documentation.
- Strong written and verbal communication skills.
- Ability to think logically and be proactive under the variable schedules of a startup site.
- Ability to work as part of a team and on own initiative in a constructive manner.
- Strong attention to detail and precision in preparing and reviewing GMP documentation.
- Previous experience in quality management systems such as Veeva, SAP, PAS-X, Delta V, Trackwise etc.
- Knowledge of industrial regulations including those of FDA, HPRA, EMEA and other authorities related to Biologics and/or Pharmaceuticals.
Desirable:
- Experience in direct interactions with regulatory agencies during site inspection.
- Previous experience working in a sterile/low bioburden environment.
Requirements
The role is required to: Participate daily on cross-functional teams to collaboratively actively to address compliance issues and achieve project milestones. Participate in and lead investigation of deviations, risk assessments and changes, ensuring appropriate actions are implemented timely. Provide QA review and approval of Change Controls, Deviations/CAPAs, SOPS and related documentation for compliance to GMP and site requirements at the facility. Provide QA oversight to GMP readiness, technical transfers, regulatory approvals and clinical operations at the facility. Assist in the development of training curricula and records for QA and providing SME training on Quality Assurance SOPs as required. Assist in the creation and maintenance of QA SOPs, metrics and reports in line with site requirements. Support an environment of continuous improvement by identifying and implementing efficiencies and quality improvements. Work collaboratively to foster strong relationships with management and colleagues and to drive a safe and compliant culture. Ensure the escalation of compliance risks to management in a timely manner. What skills you will need: In order to excel in this role, you will more than likely have: Bachelor's degree, or higher (Science/Quality/Technical). 4-5 years' experience, ideally in Quality Assurance, Quality Control or Technical Operations within the Biological and/or pharmaceutical industry. Previous experience in QRM, SQM, Deviations and Change Control, participating in investigations and problem solving. Strong attention to detail and precision in preparing and reviewing GMP documentation. Strong written and verbal communication skills. Ability to think logically and be proactive under the variable schedules of a startup site. Ability to work as part of a team and on own initiative in a constructive manner. Strong attention to detail and precision in preparing and reviewing GMP documentation. Previous experience in quality management systems such as Veeva, SAP, PAS-X, Delta V, Trackwise etc. Knowledge of industrial regulations including those of FDA, HPRA, EMEA and other authorities related to Biologics and/or Pharmaceuticals. Desirable: Experience in direct interactions with regulatory agencies during site inspection. Previous experience working in a sterile/low bioburden environment. #LI-KV1