1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
Not Disclosed by Recruiter
The job description is as below:
Purpose of the RoleTo ensure timely, accurate, compliant, and scientifically justified responses to regulatory and customer queries related to pharmaceutical and medical device testing, in alignment with global regulatory and accreditation requirements.
Key Responsibilities
1. Regulatory Query ManagementReceive, log, track, and respond to regulatory queries, including US ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
12.00 LPA TO 13.00 LPA
Position: Dy. Manager - Quality
Location: Vapi
Experience: 8 - 10 Years
Industries: Pharma API
Responsibilities:
Quality Management System (QMS)
Establish, implement, and maintain an effective Quality Management
System in line with cGMP, ICH, USFDA, EU-GMP, WHO, and other regulatory requirements.
Ensure compliance with SOPs, policies, and ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 13.00 LPA
Position: Asst. Manager/ Manager - ADL
Location: Vapi
Experience: 8 - 10 Years
Industries: Pharma - API
Responsibilities:
Analytical Development & Validation
Lead development, optimization, and validation of analytical methods for APIs, intermediates, and finished dosage forms.
Perform method validation as per ICH, USP, EP, and IP ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
6.00 LPA TO 7.20 LPA
Job Title: International Purchase & Supplier Management Executive
Role Objective
To manage end-to-end purchase activities against sales orders, ensuring timely purchase execution, commercial optimization, contractual compliance, and seamless coordination with international suppliers and internal stakeholders. The role is accountable for converting sales demand into accurate, compliant, and cost-effective purchases through SAP. ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
4.00 LPA TO 4.80 LPA
Name & Address of Organisation
Ahmedabad - 380054.Prince Industrial Park, Kuha, Ahmedabad 382433
Nature of Business
Machine Manufacturer
Total Turnover & Total Manpower
above 40
Requirement for Position (Designation)
Sr. Service Engineer
Qualification: Academic/Technical/Professional:
BE Mechnical
Exeperience in Years
5 to 6 years
Preffered Industries
Packaging Machinery
Place Of Work
Thaltej, Ahmedabad
Job description/ Nature of Work/ Job Requirement :
Service for our Bag and pouch making ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
25.00 LPA TO 26.00 LPA
Roles & Responsibilities:
Monitor SIEM Alerts on 24 x 7 x 365 basis including Night Shifts on a rotational roster.
Investigate Alerts Detected and carryout Incident Response.
Document & report appropriate Incidents to the concerned Resolver Groups using Ticketing Tools.
Monitor Network Traffic, perform Threat Hunting to identify compromised systems, negate ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Officer
Location: Bhimpore - Daman
Experience: 1 - 2 Years
Industries: Pharma
Responsibilities:
Individually handling department & manpower.
Strong leadership skills to guide, supervise work activities, and help team members develop their skills.
Work allocation / Planning and Review of documents.
Preparation of SOP, Specification, Standard Test Procedures ...
1 Opening(s)
4.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: Executive - Utility & Maintenance
Location: Vapi
Experience: 4 - 6 Years
Industries: Pharma API
Responsibilities:
Planning and execution of routine maintenance activities.
Check utility daily Log sheet.
Co- ordination with all departments pertaining to maintenance activity.
Carry out all the maintenance activities as ...
1 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Sarigam Near By Vapi
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of obsolete ...
3 Opening(s)
15.0 Year(s) To 25.0 Year(s)
15.00 LPA TO 20.00 LPA
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ...