PETTOOLS PVT LTD, Navi Mumbai a precision manufacturing tools and engineering company specializing in high-quality engineered solutions.

Key Responsibilities:

– Prepare, maintain, and manage technical documentation related to manufacturing processes.
– Handle drawings, reports, work instructions, and quality records.
– Ensure proper filing, record-keeping, and version control of engineering documents.
– Coordinate with production, quality, and design teams for document updates.
– Assist in audits and perform data entry using Microsoft Office tools.

Required Skills:

– Good knowledge of Microsoft Office (Excel, Word, PowerPoint).
– Basic understanding of mechanical drawings and engineering terminology.
– Strong organizational skills and attention to detail.
– Effective communication and coordination skills.

Preferred Skills :

– Basic knowledge of AutoCAD or design software.
– Understanding of manufacturing processes. – Microsoft Excel – Must

Benefits:

– Hands-on training in the precision engineering industry.
– Leave encashment and Paid time off.
– Provident Fund.
– Work Location: In person.

Position Details:

– Job Location: Rabale, Navi Mumbai
– Experience: Freshers are welcome
– Department: Quality Control
– Educational Qualification: Diploma / Bachelor’s Degree in Mechanical Engineering
– Duration: 2 Years Contract
– Offered CTC – 2.5-3 LPA
– Working Days – Mon – Sat
– Working Time – 8:30 AM – 6:30 PM

CREATIVE CARVE PVT LTD hiring an experienced Quality – Line Inspector to manage and monitor inspection activities on automotive production lines. The candidate should have at least 1+ year of experience in the automotive manufacturing industry and be responsible for ensuring products meet required quality standards.

The role involves working closely with production, engineering, and supervisors to improve process quality, reduce defects, and maintain product integrity.

Key Responsibilities

• In-Process Inspections: Perform routine, interval-based checks on products as they move down the assembly line to catch defects early.
• Compliance Verification: Ensure operators follow standard operating procedures (SOPs) and that mistake-proofing (Poka-Yoke) controls are working properly.
• Defect Management: Identify, document, and segregate non-conforming materials or parts to prevent them from progressing to the next stage.
• Tool Calibration: Verify that measurement equipment, gauges, and instruments are calibrated and fit for daily use.
• Reporting & Documentation: Log inspection results, generate shift reports, and input data into quality tracking databases.

Requirements:

• 0- 5 year of experience in automotive quality inspection
• Knowledge of production line inspection and quality standards
• Good coordination and reporting skills

Education:

• Diploma or Bachelor’s degree in Mechanical, Automobile, or Industrial Engineering.

Salary:₹3.5 LPA – ₹10 LPA

Benefits:

• PF
• ESIC
• PT
• Canteen Facility
• Uniform

Job Types: Full-time, Permanent

Pay: ₹35,000.00 – ₹40,000.00 per month

Benefits:

• Food provided
• Health insurance
• Leave encashment
• Provident Fund

Experience:

• Quality line inspection: 1 year (Preferred)

Work Location: Remote

Job Responsibilities:

• Provide onsite support for desktops, laptops, peripherals, and mobility devices.
• Troubleshoot Windows OS, Outlook, Office 365, VPN, hardware, and basic network issues.
• Perform AD/Azure AD user management and GPO-related updates.
• Support Intune imaging, software deployment, and compliance.
• Maintain asset inventory and coordinate with OEM/Vendor teams.
• Ensure SLA compliance and timely documentation of activities.

Desired Candidate Profile:

• Proven experience as Desktop Support Engineer / Support Technician
• Any Graduate can apply
• Minimum 1 year of experience required in MNC environment
• Good communication and interpersonal skills

Company: CMS IT Services (Mahape Office),Rupa Solitaire, F wing, lift no 22 & 23, 13th floor, Millennium Business Park, Mahape,Navi Mumbai, Maharashtra, India – 400710

Pay: ₹235,000.00 – ₹300,000.00 per year

Benefits:

• Health insurance
• Leave encashment
• Life insurance
• Provident Fund

Site : Airoli

Experience : 5/8 years

Key Responsibilities

• Supervise labour, contractors, and subcontractors at site.
• Ensure construction work follows approved drawings, specifications, and BOQ.
• Check quality of materials and workmanship.
• Monitor RCC, masonry, plastering, flooring, finishing, and other civil works.
• Coordinate with engineers, architects, contractors, and vendors.
• Allocate daily work to workers and monitor productivity.
• Check measurements and progress of completed work.
• Ensure proper use of materials and minimize wastage.
• Maintain daily site reports, labour attendance, and work-progress records.
• Ensure compliance with safety rules and PPE requirements.
• Identify site issues and report them to the Project/Site Engineer.
• Monitor work against the project schedule and deadlines.
• Coordinate material requirements and deliveries.

QA Engineers : 5 Post

Technical Recruiters : 4 Post

Instructions:

SC/ST/OBC (NCL-Non-Creamy Layer) candidates applying for Unreserved (UR) seats shall be considered subject to their fulfilling the standards applicable to candidates belonging to General category.

Candidates need to LOGIN to the respective NATS/NAPS portal using their User ID/Email ID and APPLY for the apprenticeship Openings/Opportunities with the Establishment ID of Indian Oil Corporation Limited (Marketing Division)-Western Region

• NATS – WMHMCC000053
• NAPS – E01172700332

Applicants are strictly required to submit their applications only against the vacancies notified under the states of Western Region (Maharashtra, Gujarat, Goa, Madhya Pradesh, Chhattisgarh, UT of Daman & Diu, UT of Dadra & Nagar Haveli). Allocation of training locations shall be restricted exclusively to the states specified therein. Selection of training locations outside the notified states in the application portal shall not be entertained and will result in rejection of the application. This condition shall be binding for the engagement process of apprentices under Western Region.

Other Requirements: 

• Candidate should have a PAN Card
• Candidates should have an Aadhaar Card
• Candidates should have a Bank Account & Cheque Book with their names printed
• Candidates should have scanned copy of Educational Qualification Certificates

How to Apply:

Candidates meeting the prescribed eligibility criteria may apply online through NAPS/NATS Portal (as mentioned in F-2) from 10.2026 (10:00 A.M.) to 04.11.2026 (5.00 P.M.) NO other means / mode of application shall be accepted other than what is mentioned above in this advertisement. Candidates must ensure that they have successfully applied for the relevant post through respective NATS / NAPS portal within stipulated timeline.

Click on APPLY to get Official Notification

Designation: QA Officer
Reporting To: Assistant Manager / Manager – QA
Industry: Pharmaceutical / API Manufacturing
Experience: 2–5 Years
Employment Type: Full-Time
Location: Turbhe

1. Job Purpose

To perform day-to-day Quality Assurance activities and ensure that manufacturing, documentation, testing, and other operational activities comply with GMP requirements, approved SOPs, specifications, regulatory requirements, and company quality standards.

2. Key Responsibilities A. Shop-Floor QA & GMP Compliance

• Monitor manufacturing and packing activities to ensure compliance with approved SOPs and GMP requirements.
• Perform routine shop-floor inspections and verify compliance with GMP practices.
• Check line clearance before commencement of manufacturing/packing activities.
• Monitor critical process parameters and in-process activities.
• Verify equipment status, area cleanliness, environmental conditions, and material status.
• Report and escalate GMP deviations and quality issues to the QA supervisor/manager.

B. Batch Documentation

• Review BMRs, BPRs, logbooks, checklists, and other manufacturing documents for completeness and accuracy.
• Ensure entries are made as per Good Documentation Practices (GDP).
• Verify corrections, signatures, dates, and traceability of records.
• Identify documentation discrepancies and coordinate with concerned departments for correction.

C. Quality Management System

• Support handling of deviations, CAPA, change controls, OOS/OOT, complaints, and other quality events.
• Assist in investigation and root-cause analysis.
• Track assigned CAPA and change-control activities.
• Maintain QA records and quality documentation.
• Support implementation and monitoring of QMS procedures.

D. Sampling & Material/Finished Product Activities

• Perform or coordinate sampling of raw materials, packaging materials, intermediates, and finished products as per approved procedures.
• Verify material status labels and storage conditions.
• Coordinate with QC for sample submission and testing.
• Ensure proper status identification of materials and products.

E. Document Control

• Issue and control SOPs, formats, logbooks, and other controlled documents.
• Ensure obsolete documents are withdrawn from use.
• Maintain controlled-copy records as applicable.
• Support periodic review and revision of QA documents.

F. Audit & Inspection Support

• Support preparation for internal audits, customer audits, and regulatory inspections.
• Participate in GMP audits and inspections.
• Provide required QA documentation and records during audits.
• Assist in tracking and closing audit observations.

G. Training

• Participate in GMP, SOP, GDP, data integrity, and other quality-related training.
• Support training of production and QA personnel on applicable SOPs.
• Maintain training records and ensure completion within defined timelines.

H. Validation & Qualification Support

• Assist QA in review and execution of validation and qualification activities.
• Support review of protocols and reports related to equipment qualification, process validation, cleaning validation, and other validation activities.
• Ensure activities are performed according to approved protocols.

3. Daily QA Activities

• Perform manufacturing area/shop-floor checks.
• Verify line clearance.
• Review manufacturing documentation.
• Check equipment and area status.
• Monitor GMP compliance.
• Verify material/product status.
• Record and report deviations.
• Coordinate with Production and QC on quality-related issues.
• Ensure proper documentation and data integrity.

4. Key Performance Indicators (KPIs)

• Timely completion of batch record review.
• Compliance with GMP and GDP requirements.
• Timely reporting and documentation of deviations.
• Timely completion of assigned CAPA/change controls.
• Accuracy of QA documentation.
• Audit and inspection readiness.
• Training compliance.
• Reduction in documentation errors and recurring GMP observations.

5. Educational Qualification

Essential:

• B.Pharm / M.Pharm / B.Sc. / M.Sc. in Chemistry, Life Sciences, or a related field.

6. Experience

• 2–5 years of relevant experience in Quality Assurance, preferably in pharmaceutical/API manufacturing.
• Experience in GMP documentation, shop-floor QA, batch record review, deviations, CAPA, and change control will be preferred.

7. Technical Knowledge

• Basic to good knowledge of cGMP and GDP.
• Understanding of pharmaceutical/API manufacturing processes.
• Knowledge of:
• BMR/BPR review
• Line clearance
• Shop-floor QA
• Deviations
• CAPA
• Change Control
• OOS/OOT
• Data Integrity
• Document Control
• GMP Audits
• Basic knowledge of validation and qualification activities.

8. Required Competencies

• Attention to detail
• Good documentation

KEY RESPONSIBILITIES

• Identify and develop new business opportunities
• Generate leads and build a strong client pipeline
• Develop and maintain long-term client relationships
• Conduct regular follow-ups with prospective and existing clients
• Achieve assigned sales targets and business objectives
• Coordinate with internal teams to ensure excellent client service

LANGUAGE SKILLS

Candidates with proficiency in English, Hindi, Marathi, Tamil, Telugu, Malayalam, Kannada, Gujarati, Punjabi and other Indian languages are welcome to apply.

WHAT WE OFFER

Competitive Salary | Performance Incentives | Professional Growth | Career Development

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How to Apply

• Update your profile from Dashboard
• Read Job description and eligibility criteria carefully.
• Interested and eligible candidates may click on APPLY to process online application.

Location: Karjat, Maharashtra
Employment Type: Full-Time, In-Person
Shift Duration: 8-hour shifts
Salary Range: ₹25,000 – ₹30,000 per month (based on experience)
Reporting To: Resident Medical Officer

Job Summary:

We are seeking a dedicated and compassionate Resident Medical Officer (RMO) to join our multidisciplinary healthcare team at our Karjat center. The RMO will play a critical role in the medical management of psychiatric and de-addiction patients, including clinical assessments, treatment planning, medication oversight, emergency care, and overall medical operations. You will work collaboratively with psychiatrists, psychologists, counsellors, and nursing staff to provide integrated, patient-centred care.

Key ResponsibilitiesClinical Management & Patient Care:

– Conduct thorough physical and mental health evaluations of all admitted patients

– Develop and implement personalized treatment plans in collaboration with the psychiatric and clinical team

– Manage and monitor patient medications, dosing adjustments, and potential side effects

– Assess patient medical history, vital signs, and overall health status

– Maintain clinical responsibility for patient care when and as required

Emergency & Crisis Management:

– Provide immediate emergency medical care and stabilization

– Manage acute psychiatric or addiction-related crises

– Handle medical complications arising during treatment

– Ensure prompt response to patient medical emergencies

Daily Operations & Leadership:

– Conduct center rounds and monitor day-to-day medical functions thoroughly

– Oversee medical records management and patient documentation

– Coordinate with multidisciplinary staff to ensure seamless care delivery

– Maintain accurate, confidential, and compliant medical records

– Contribute to the overall development and improvement of the healthcare team

Administrative Support:

– Support administrative functions of the center

– Assist in regulatory and compliance matters

– Participate in quality assurance and patient safety initiatives

– Contribute to clinical audits and performance improvements

Training & Development:

– Receive comprehensive training on Calida Rehab protocols and procedures

– Participate in ongoing professional development programs

– Share knowledge and mentor junior clinical staff where applicable

– Stay updated with latest medical and psychiatric care practices

Adherence to Standards:

– Adhere strictly to regulatory and ethical standards in patient care

– Maintain confidentiality and patient privacy at all times

– Follow hospital protocols, infection control measures, and safety guidelines

– Ensure compliance with Maharashtra Medical Council regulations

Required QualificationsEducation & Licensing (Mandatory):

• – Bachelor’s Degree in Medicine: BHMS (Bachelor of Homeopathic Medicine) / BAMS (Bachelor of Ayurvedic Medicine) / MBBS (Bachelor of Medicine, Bachelor of Surgery)
• – Valid Maharashtra State Medical Registration: Must possess active registration with Maharashtra Medical Council (MMC)

Experience:

• Minimum 2-3 years of relevant medical experience in any field
• Experience in psychiatry, de-addiction, or mental health care is preferred but not mandatory
• Proven skills in emergency medical management and critical patient care

Professional Skills:

• Strong clinical assessment and diagnostic abilities
• Excellent medication management and prescribing knowledge
• Proficiency in emergency medical protocols and crisis intervention
• Strong communication skills – both written and verbal
• Ability to work effectively in a multidisciplinary team environment
• Strong organizational and time-management abilities
• Commitment to patient-centred, compassionate care

Work Requirements:

• Ability to work 8-hour shifts on a consistent, rotating basis
• Flexibility to work at either Karjat or Pune center as per organizational needs
• Willingness to be on-call for emergencies when scheduled
• Ability to maintain composure in high-stress situations

Benefits & CompensationSalary & Compensation:

• Monthly Salary: ₹25,000 – ₹30,000 (based on qualifications and experience)
• Benefits Package
• Provident Fund (PF): Statutory PF contribution as per government regulations
• Accommodation: Free residential accommodation provided at the center
• Food & Meals: Complimentary meals and nutritious food throughout duty
• Comprehensive Training: Professional training on Calida Rehab protocols, psychiatric care, and de-addiction treatment
• Career Development: Opportunities for professional growth within the organization
• Supportive Work Environment: Collaborative team of experienced healthcare professionals

Working Conditions:

• Location: Karjat center (with possibility of deputation to Pune center)
• Shift Pattern: 8-hour fixed shifts (day/evening/night rotation)
• Environment: Residential rehabilitation center with in-patient facilities
• Nature of Work: Clinical, administrative, and emergency medical care
• Work Culture: Multidisciplinary team approach with emphasis on patient welfare

Application Process:

How to Apply:

• Login and ensure your profile is updated with all necessary information.
• Read above details carefully for eligibility criteria.
• Interested and eligible candidates may click on apply to process online application.
• Shortlisted candidate may get revert within seven working days.