1 Opening(s)
3.0 Year(s) To 8.0 Year(s)
0.00 LPA TO 10.00 LPA
Position Name: Quality Engineer – Pole FabricationLocation: OmanNationality Preferred: IndianExperience Required: 3+ YearsSalary Range: 450 – 500 OMR (CTC)
Job Summary:
We are looking for an experienced Quality Engineer with expertise in Pole Fabrication / Manufacturing to oversee quality assurance and quality control activities, ensure compliance with standards, and drive continuous improvement in production processes. The ideal candidate should have strong ...
1 Opening(s)
5.0 Year(s) To 9.0 Year(s)
Not Disclosed by Recruiter
Job Summary
Seeking experienced Business Development / Sales Managers for project-based B2B sales in the wallcoverings and interior solutions segment. The role involves managing end-to-end sales activities, building strong relationships with architects and interior designers, and driving business growth within commercial projects.
This is an individual contributor role with direct reporting to ...
1 Opening(s)
1.5 Year(s) To 2.0 Year(s)
3.00 LPA TO 3.60 LPA
Role Summary
The Digital Marketing Specialist will be responsible for managing and optimizing end-to-end digital marketing activities to generate qualified leads, improve conversion rates, and strengthen brand presence. The role requires a mix of analytical thinking, execution capability, and performance-driven mindset.
KRA: Task / Activities
Conduct structured competitor analysis (SEO, paid ads, messaging, ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
4.20 LPA TO 4.80 LPA
Role Summary:
We are seeking a results-driven SEO Specialist with 2.5–3 years of experience to improve website rankings, drive organic traffic, and enhance online visibility. The candidate will be responsible for on-page, off-page, and technical SEO activities aligned with business goals.
KRA: Task / Activities
Conduct keyword research and competitor analysis to identify ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 6.00 LPA
Supervise day-to-day QC laboratory activities (chemical, instrumental, and microbiology where applicable).
Review and approve analytical results, COAs, test reports, and raw data.
Ensure compliance with cGMP, GLP, ICH, and regulatory guidelines (USFDA, EMA, WHO, etc.).
Oversee calibration, qualification, and maintenance of instruments (HPLC, GC, FTIR, UV, KF, etc.).
Review and update SOPs, STPs, GTPs, ...
2 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 3.00 LPA
Job Summary
27.04.26
131944
HPS/2026/362
Production/Quality Supervisor
Male
2
1 to 3
B.Pharma/M.Pharma
Masat
We are seeking a proactive and responsible Production / Quality Supervisor with 1–3 years of experience in the pharmaceutical industry. The candidate will oversee daily production or quality operations, ensure compliance with GMP standards, and maintain smooth workflow within the department.
Key Responsibilities
Production:
Supervise daily manufacturing activities as ...
3 Opening(s)
0 To 1.0 Year(s)
1.80 LPA TO 1.80 LPA
Job Description
27.04.26
131943
HPS/2026/361
Trainee Production/Quality
Male
3
0 to 1
B.Pharma/M.Pharma
Masat
Job Summary
We are looking for enthusiastic and detail-oriented freshers or candidates with up to 1 year of experience to join our Production and Quality departments as Trainees. The role offers hands-on exposure to pharmaceutical manufacturing processes and quality systems in a regulated environment.
Key Responsibilities
Production:
Assist in manufacturing ...
4 Opening(s)
2.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 4.80 LPA
Key Requirements Experience: 2–4 years in accounting role Education: B.Com / M.Com (MBA Finance is a plus) Strong hands-on experience in Tally (ERP/Prime) Working knowledge of GST, TDS, and taxation Good understanding of accounting principles Proficiency in MS Excel Strong attention to detail and organizational skills
Key Responsibilities Handle day-to-day accounting ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: Manager - QA
Location: Kadi - Ahmedabad
Experience: 5 - 7 Years
Industries: Pharma
Responsibilities:
Quality Assurance & Compliance
Ensure compliance with cGMP, GLP, and regulatory requirements (WHO, USFDA, MHRA, etc.)
Handle audits (internal, external, regulatory) and ensure audit readiness at all times
Review and approve SOPs, BMRs, BPRs, protocols, and reports
Documentation Management
Oversee preparation, ...
5 Opening(s)
2.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
📋 Documentation & Compliance
Preparation, review, and control of SOPs, BMRs, BPRs, and other GMP documents
Ensure proper documentation practices (GDP compliance)
Handling change control, deviation, and CAPA
🏭 Shop Floor QA Activities
Line clearance before batch initiation
In-process checks and verification
Monitoring of manufacturing and packing activities
🧪 Validation & Qualification
Support in process validation, cleaning validation
Equipment qualification ...