Scott Edil Walk-in IPQA, QA, QC, Production, IT.
- Company Overview
- Job Role & Responsibilities
- IPQA / QA / QMS Roles
- Quality Control (QC)
- Microbiology
- DPI & OSD Production
- Engineering
- IT
- Warehouse
- Eligibility / Qualifications
- Required Education (Relevant Courses)
- Location & Salary
- Application Process
- Why Consider Scott Edil for Your Pharma Career
- Frequently Asked Questions (FAQs)
- Is this walk-in drive open to freshers?
- Is EU regulatory experience mandatory?
- Can candidates from outside Chandigarh apply?
- What documents should I carry for the walk-in?
- Is this a permanent role?
- Summary Table
B.Pharm/M.Pharm EU Regulatory Vacancies – Scott Edil Chandigarh
Scott Edil hiring 39 professionals for EU regulatory roles in Chandigarh. IPQA, QA, QC, Production, IT. Walk-in 08 Feb 2026.
Scott Edil is conducting a large-scale walk-in hiring drive focused on EU regulatory operations at its Chandigarh facility. This opportunity is targeted at experienced pharmaceutical professionals who have worked directly with regulated markets such as the European Union, MHRA, and PIC/S. The drive is designed to strengthen Scott Edil’s quality, manufacturing, and compliance teams supporting global regulatory missions. Candidates with strong exposure to IPQA, QMS, Quality Assurance, Quality Control, Production, Engineering, Microbiology, IT, and Warehouse operations are encouraged to attend.
This hiring initiative reflects Scott Edil’s continued expansion in regulated pharmaceutical manufacturing and its long-term commitment to high-quality, compliant healthcare products for global markets.
Company Overview
Scott Edil is a well-established pharmaceutical manufacturing company known for delivering compliant, patient-focused formulations across domestic and international markets. Operating with the philosophy of “Complementing Life,” the company has built a strong reputation for quality-driven manufacturing, regulatory compliance, and continuous improvement.
Scott Edil’s facilities are designed to meet stringent international regulatory standards, including EU GMP, MHRA, and PIC/S guidelines. The organization places a strong emphasis on data integrity, quality systems, risk management, and regulatory readiness. Its operations span multiple dosage forms, including Oral Solid Dosage (OSD) and Dry Powder Inhalation (DPI), supported by robust quality and engineering teams.
Working at Scott Edil means being part of a regulated pharma environment where compliance, patient safety, and professional growth are taken seriously. The company provides exposure to international audits, advanced quality systems, and cross-functional collaboration, making it an attractive employer for experienced pharma professionals.
Job Role & Responsibilities
Scott Edil is hiring across multiple departments to support EU regulatory missions. All roles require hands-on experience with regulated markets and strong understanding of GMP, documentation, and audit readiness.
IPQA / QA / QMS Roles
Professionals in IPQA and QA will play a critical role in ensuring compliance with EU GMP requirements across manufacturing operations.
Key responsibilities include:
- In-process quality assurance activities for regulated products
- Review and approval of batch manufacturing records and critical process parameters
- Implementation and maintenance of Quality Management Systems (QMS)
- Handling deviations, CAPA, change controls, and risk assessments
- Preparation and support for EU, MHRA, and PIC/S regulatory audits
- Ensuring data integrity and compliance with ALCOA+ principles
- Cross-functional coordination with production, QC, and engineering teams
These roles are ideal for candidates with strong regulatory exposure and the ability to manage quality systems in a high-compliance environment.
Quality Control (QC)
QC professionals will be responsible for analytical testing and release of regulated pharmaceutical products.
Key responsibilities include:
- Raw material, in-process, and finished product testing
- Stability studies and documentation as per EU guidelines
- Handling analytical instruments and laboratory compliance
- Review of analytical data and investigation of OOS/OOT results
- Supporting regulatory inspections and audit responses
Strong knowledge of pharmacopeial standards and EU regulatory expectations is essential for these positions.
Microbiology
Microbiology roles support sterile and non-sterile operations through environmental and microbiological monitoring.
Responsibilities include:
- Environmental monitoring of manufacturing areas
- Water system analysis and microbial testing
- Media preparation, validation, and documentation
- Support for regulatory audits and compliance activities
These positions are critical for maintaining microbiological control in regulated manufacturing environments.
DPI & OSD Production
Production roles focus on manufacturing of Oral Solid Dosage and Dry Powder Inhalation products for regulated markets.
Responsibilities include:
- Operation and supervision of production processes as per EU GMP
- Equipment handling, line clearance, and process documentation
- Coordination with IPQA and QC teams
- Ensuring adherence to SOPs, safety, and compliance standards
Experience in regulated pharma production environments is mandatory.
Engineering
Engineering professionals ensure equipment reliability and compliance with regulatory standards.
Responsibilities include:
- Preventive and breakdown maintenance of pharma equipment
- Qualification and validation support
- Utilities management and documentation
- Regulatory audit readiness and compliance support
IT
IT roles support data integrity, system compliance, and infrastructure for regulated operations.
Responsibilities include:
- IT system maintenance in GMP environments
- Data integrity and access control management
- Support for computerized system validation (CSV)
- Regulatory compliance for IT systems
Warehouse
Warehouse professionals ensure compliant material management.
Responsibilities include:
- Raw material and finished goods handling as per GMP
- Inventory control and documentation
- Coordination with QA for material release
- Compliance with EU storage and traceability requirements
Eligibility / Qualifications
- Minimum 5 to 10 years of experience in the relevant department
- Mandatory hands-on experience with EU, MHRA, and PIC/S regulatory environments
- Strong knowledge of GMP, QMS, and data integrity
- Ability to face and support international regulatory audits
Required Education (Relevant Courses)
B.Pharmacy, M.Pharmacy, B.Sc, M.Sc, Microbiology, Biotechnology, Biochemistry, Pharmaceutical Chemistry, Pharmaceutical Analysis, Diploma in Pharmacy, Engineering (Mechanical/Electrical), B.Tech, M.Tech, Computer Science, Information Technology
Location & Salary
Job Location: Chandigarh
Interview Address:
28/06, Industrial Area Phase-2,
Chandigarh – 160002
Salary:
Salary will be offered as per industry standards and will be commensurate with experience, skill set, and regulatory exposure. Competitive CTC packages are available for EU regulatory professionals.
Application Process
This is a direct walk-in interview.
Walk-In Date: 08 February 2026 (Sunday)
Eligible candidates are requested to attend the interview in person with updated CV, relevant documents, and proof of regulatory experience.
Candidates who are unable to attend may share their CV via email:
Contact Numbers:
8628840040, 7807934034
Why Consider Scott Edil for Your Pharma Career
- Exposure to EU, MHRA, and PIC/S regulatory audits
- Stable organization with strong compliance culture
- Opportunities in regulated pharma manufacturing
- Competitive salary and professional growth
- Direct contribution to global healthcare supply chains
Frequently Asked Questions (FAQs)
Is this walk-in drive open to freshers?
No. This hiring drive is strictly for professionals with 5 to 10 years of relevant experience in regulated pharma environments.
Is EU regulatory experience mandatory?
Yes. Hands-on experience with EU, MHRA, or PIC/S audits and compliance is mandatory.
Can candidates from outside Chandigarh apply?
Yes. Candidates from any location can attend the walk-in interview if they meet eligibility criteria.
What documents should I carry for the walk-in?
Updated CV, educational certificates, experience letters, and any regulatory audit exposure documents.
Is this a permanent role?
Yes. These are full-time, on-roll positions at Scott Edil.
Summary Table
| Category | Details |
|---|---|
| Company | Scott Edil |
| Vacancies | IPQA – 05, QA – 05, QC – 05, Microbiology – 03, DPI Production – 03, OSD Production – 05, IT – 05, Warehouse – 03, Engineering – 05 |
| Required Education | B.Pharm, M.Pharm, B.Sc, M.Sc, Microbiology, Biotechnology, Biochemistry, Pharmaceutical Analysis, Engineering, IT |
| Experience | 5 to 10 years with EU, MHRA, PIC/S exposure |
To apply for this job email your details to hr.searle@scott-edil.com
