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1 - 3 years

5 - 10 Lacs

Hyderabad

Work from Office

Job Summary We are seeking a dynamic and experienced Production Shift Chemist in Active Pharmaceutical Ingredient (API) to support the development of robust and cost effective API's by executing scale up batches for all new and existing APIs at GMP Kilo Lab. Roles & Responsibilities You will be responsible for Equipment Operations of Reactors (GL, SS & All Glass), Mobile Receivers & tanks, ANFD, PNF & VTD, Isolators (Reactor Charging, ANFD Discharge, Dispensing/packing, sifter & multimill), Air jet mill, Multimill, Blender & Sifter, Spray dryer, TCU, Vacuum Pumps, AODD Pumps, centrifugal pumps & peristatic pumps, VNS sealing machine, RLAF & dispensing booth, Refrigerators and Deep freezers etc. You will be responsible to Execution of Batches, Equipment product change over & General cleaning of equipment. Batch production record filling as per SOP & as per Good documentation practices. You will be responsible for Filling of Equipment Logs, daily production monitoring records like Temperature, Humidity & RH, weighing balance calibrations, reviewing of house keeping records, Printing Data logger records and Updating status boards etc as per site SOPs. Collection of Records/books, submission of completed BPRs/Records to QA. You will be responsible for In process sample collection from Reactors, ANFD & VTD etc. Raw Material, Solvents handling, material moments & dispensing and maintaining records as per SOP. You will be responsible to reduce the accidents in the plant by following safety principles, install earth rods to remove static electricity from material, Handling different chemicals with appropriate PPE & following SHE Norms. Monitor adherence of behavioral safety of contract persons. You will be responsible to meet the production schedules and reduce breakdowns by planning the equipment for idle condition to prepare for preventive maintenance, issue work order to maintenance to carry on with maintenance, follow up with maintenance on problem rectification. You will be responsible for Handling of Production waste & Detoxification batches execution. Support the engineering team in equipment qualification activities to meet the batch planning. You will be responsible for handling, initiation of deviations, incidents and support for closure of deviation & Incident reports Qualification Educational qualification: B.Sc Chemistry, M.Sc Chemistry & Diploma in Chemical engineering Minimum work experience: 2-6 years of experience in Pharma industry Skills & attributes: Technical Skills Experience on Process of Product Development Knowledge in API chemical Process & equipment. Knowledge of unit operations. Knowledge in Safety, Health and Environment guidelines (SHE) guidelines. Experience in data entry in SAP system. Behavioural Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

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2 - 7 years

2 - 7 Lacs

Hyderabad

Work from Office

Walk In Drive For Production Injectables In Formulation Division @ Corporate Office Department:- Production Injectables Qualification :- Diploma | ITI | B Tech | B Pharmacy | BSc | MSc | M Pharmacy Experience :- 2 to 8 Years Division :- Formulation Interview Date:-10-05-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur & MSNF-V, RK Puram Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

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3.0 - 8.0 years

5 - 12 Lacs

pune

Work from Office

Role & responsibilities * Design and Development for Trims components (Interior or Exterior) or BIW or Closure (Sealing, Doors, Tailgate) components. Preferred candidate profile * 3 to 10 years experienced candidates either with Interior or Exterior Trims experience or in BIW or Closures (Sealing, Doors, Tailgate) components experience. * Good working experience in CATIA tool. * Preferring BE or Diploma candidates. * Looking for candidates who can join immediately or by max 30 days notice. Interested candidates can share their resumes to raghul.ramesh@hindujatech.com

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0.0 - 4.0 years

2 - 5 Lacs

anklesvar, ankleshwar

Work from Office

Multiple positions open for various operators who are responsible to operator vial filling/ sealing machine, autoclave, ampoule filling machine, manufacturing of injectable.

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5.0 - 10.0 years

8 - 18 Lacs

pune

Work from Office

Experience in Sealing and Glasses Design & Development at Automobile OEM around 8 to 15 years of experience. (Door, Tailgate & Hood) Collaborate with cross-functional teams including Body-in-White (BIW), Door Trim and Vehicle Integration to ensure sealing and glass system compatibility and performance. Must have hands on experience in automobile domain having worked on BIW closure (Door, Tailgate & Hood) systems and their subsystem designs. Interface with suppliers for glass tooling, lamination, tempering, and encapsulation processes . Ensure compliance with regulatory and internal standards for water tightness, air leakage, dust ingress, and NVH Strong knowledge of EPDM, TPV, TPE materials , extrusion/molding processes and optical distortion assessments Candidate should be experienced in Catia and PLM softwares like Team center. Sound knowledge of engineering and system documents like DFMEA, DVP, DFA etc. Good technical knowledge of automotive Sheet metal parts, manufacturing and assembly -process. Should be able to prepare & deliver presentations of the concepts/master section. Should be able to do tolerance stack up & GD&T added advantage. Hand on experience in Part development/supplier interaction added advantage.

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15.0 - 24.0 years

15 - 25 Lacs

ahmedabad, vadodara, mumbai (all areas)

Work from Office

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 1 to 25 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile No of Openings Officer - 30 Senior Officer - 16 Executive - 4 Assistant Manager - 4 Manager - 2 AGM / DGM / GM - 1 Share with Your Colleagues & Seniors Free Job Placement Project Expansion on going

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15.0 - 24.0 years

15 - 25 Lacs

bharuch, dahej, ankleshwar

Work from Office

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 1 to 25 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755486 Free Job Required Candidate profile No of Openings Officer - 30 Senior Officer - 16 Executive - 4 Assistant Manager - 4 Manager - 2 AGM / DGM / GM - 1 Share with Your Colleagues & Seniors Free Job Placement Project Expansion on going

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2.0 - 7.0 years

2 - 6 Lacs

bharuch, dahej, ankleshwar

Work from Office

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755967 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

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2.0 - 7.0 years

2 - 6 Lacs

ahmedabad, vadodara, mumbai (all areas)

Work from Office

Interview for SVP & Injectable Pharma Formulation Plant in Bharuch on Company / Permanent Payroll Experience: 2 to 6 Yrs CTC: As per industry Work Location: Dahej Send CV on sdpbharuch@gmail.com with Subject: SVP Bharuch & Call 9727755967 Free Job Required Candidate profile Autoclave Operator Granulation Operator Mixing Operator Grinding Operator Cartonator Operator Washing Tunnel Operator Ampoule Filling Operator Vial Filling Operator Vial Sealing Operator Lyo Operator

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1.0 - 6.0 years

1 - 3 Lacs

asansol

Work from Office

Cleaning, disinfecting, sterilizing, and distributing surgical instruments and medical equipment. Ensures proper functioning of sterilization processes, maintains hygiene standards, and follows infection control protocols.

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7.0 - 12.0 years

25 - 35 Lacs

gurugram

Remote

Job Title: Senior Data & Network Management Engineer Location: Remote Job Type: 6 months contract Shift: 2 to 11 pm IST Notice: Immediate to 15 days max Reports to: Principal Architect, Network Management Must-have qualifications 7+ years building data-centric backend services in Java, Kotlin, Go, or Python . Hands-on mastery of SNMP architecture (MIB design, getters/setters, traps, security models, typical NOC workflows). Proven experience designing schemas (Avro, Protobuf, JSON Schema, or GraphQL) and evolving them in production. Built and operated streaming pipelines (Kafka, Pulsar, or Flink/Spark Streaming) handling >1 k msgs/s. Solid grasp of network-management concepts : fault & performance monitoring, polling vs trap models, L2/L3 basics. Comfort with containerized deployments (Docker / Kubernetes) and IaC (Terraform/Helm). Excellent documentation & cross-team communication skills. Nice-to-haves Experience integrating NETCONF/YANG, gNMI, or TR-069 alongside SNMP. Familiarity with OpenTelemetry , Prometheus exporters, and Grafana dashboards. Prior work on device-side agents or embedded Linux. Knowledge of AMI / utility metering networks. Exposure to domain-driven design and event-sourcing patterns. What we offer Impact: Green-field architecture with real-world scale in critical infrastructure. Autonomy: Direct input into technical strategy and tool selection. Culture: Kindness-powered problem solving, low-ego collaboration, continuous learning. Competitive compensation, flexible work schedule, and professional-development stipend.

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2.0 - 7.0 years

5 - 10 Lacs

visakhapatnam

Work from Office

Job Role: Junior Associate to Senior Associates Manufacturing (Injectables) Eligibility criteria: Qualification: Any Diploma/BSc/B.Pharma/MSc/M.Pharma Years of Experience: 2 to 10 Years should be from injectable manufacturing plant. Job Description Operate production equipment such as Injectable , Sterile , Parenteral machines, Vial / Ampoule filling , Capping , Compounding , Washing ,Sealing, Terminal sterilization, Stopper process & Visual inspection. Monitor and control the production process to ensure quality products are produced within specified parameters. Maintain accurate records of production data and perform routine maintenance tasks on equipment as required. Collaborate with other team members to resolve issues and improve overall efficiency. Ensure adherence to Good Manufacturing Practices (GMP) guidelines. Must have experience with USFDA regulatory environment & process.

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