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Life at Leben Life Sciences
We believe that employees with the right skills & attitude act as a catalyst in the organizational growth & development. We have a well defined
organizational structure comprising of experienced & qualified employees. We provide most conducive atmosphere through ambience, amenities
& appreciation to motivate employees to give their best. One of the most distinguishing characteristic to Leben is the strong bonding within its
employees. Various events like Annual Day, Ganesh Utsav, Dashera Pooja, Annual Conference etc. instills employees with enthusiasm & nurtures
team spirit. We believe in continuous training & organize several training workshops from time to time of veteran mentors.
In our growth journey, we are always on lookout for employees with integrity who are capable to take higher responsibilities & deliver above expectations. Being a growing company, we believe in internal employees taking up higher responsibilities which match your aspirations & professional growth. If you are up for it, you can apply for suitable openings as given below. Alternatively, you can mail your resumes on career@lebenlifesciences.com
Current Opening
Minimum experience required in this position:
2 years
Description:
Roles & Responsibilities :-
- Doing market analysis and research for developing new products and launching new products.
- Working in the Field to evaluate effectiveness of Strategies and formulate new strategies, monitor & motivate field staff.
- Training and development of Field Staff.
- Creating Artwork in conjunction with artist including conceptualizing, copywriting, designing of leave behinds, literatures, and packing materials such labels/cartons visual aids, etc.
- Formulating promotional/ marketing strategies for products and evaluating the effectiveness of the same.
- Understanding the basic requirements of artworks for packing material.
- Making action plans for each quarter as per the new strategies.
- Developing motivational activities and new innovative product ideas.
- Sourcing of competitors, references, strategies, etc.
- Overseeing systems in office for monitoring and improve sales performance of field and products.
- Planning & implementation of product strategy to achieve pre-determined sales for the brand assigned.
- Planning, Designing & Executing Marketing Strategies to provide the sales team with the necessary technical expertise to enable them to sell the product. This involves printed and electronic promotional material, product training, relevant clinical papers etc.
- Doing Fieldwork to understand the market, strategy implementation & Competitor's activities. Actively participating in meetings.
- Assisting the development of the annual marketing plan and for controlling advertising, promotion and sales aids in accordance with the annual marketing plan.
- Advertising agency regarding the product campaign including journal advertising, direct mail and conferences.
- Participating in Monthly sales data analysis, reports generation & preparing product forecasts.
- Communicating with the field force to assess the response to and suitability of current promotional material and to ensure that the printed promotional material is being used optimally.
- Reviewing product data to ensure that the field force is kept up to date on new developments regarding the companies or competitors&rsquo products.
- Acting as point of first reference for all product related enquiries.
- Following instructions given by HOD.
Highest Qualification :-
B.Pharm/ M.Pharm/ B.Sc/ M.Sc- MBA (Marketing)
Location :-
Akola
Minimum experience required in this position:
5+ years
Description:
Roles & Responsibilities :-
- Develops and maintains a human resources system that meets top management information needs.
- Recruits, interviews, tests, and selects employees to fill vacant positions. Ensure Man force Adequacy is maintained and attrition is maintained in desired limits.
- Plans and conducts new employee orientation to foster positive attitude toward Company goals.
- Analyzes wage and salary reports and data to determine competitive compensation plan.
- Coordinates management training in interviewing, hiring, terminations, promotions, performance review, safety, and sexual harassment.
- Advises management in appropriate resolution of employee relations issues.
- Responds to inquiries regarding policies, procedures, and programs.
- Administers performance review program to ensure effectiveness, compliance, and equity within organization. Administers salary administration program to ensure compliance and equity within organization.
- Administers benefits programs such as life, health, and dental insurance, pension plans, vacation, sick leave, leave of absence, and employee assistance.
- Investigates accidents and prepares reports for insurance carrier. Coordinates Safety Committee meetings and acts as Safety Director. Prepares budget of human resources operations.
- Prepares employee separation notices and related documentation, and conducts exit interviews to determine reasons behind separations.
- Prepares reports and recommends procedures to reduce absenteeism and turnover.
- Represents organization at personnel-related hearings and investigations.
- Contracts with outside suppliers to provide employee services, such as temporary employees, search firms, or relocation services.
- Ensuring FDA compliances for the company.
- Identifies legal requirements and government reporting regulations affecting human resources functions and ensures policies, procedures, and reporting are in compliance. Studies legislation, arbitration decisions, and collective bargaining contracts to assess industry trends.
- Oversees the analysis, maintenance, and communication of records required by law or local governing bodies, or other departments in the organization.
- Consults legal counsel to ensure that policies comply with federal and state law.
- Writes directives advising department managers of Company policy regarding equal employment opportunities, compensation, and employee benefits
Highest Qualification :-
MBA-HR
Location :-
Akola
Minimum experience required in this position:
4+ years
Description:
Roles & Responsibilities :-
- Working on Formulation & Development of dosage forms like Oral Solids (Tablet & Capsules) &ndash IR tablets, Sustained release tablets, extended release tablets, Bilayer tablets, Capsule etc. & External preparations like Gels, Pastes, Creams, Ointments etc. under guidance of consultant.
- Working under guidance of consultant, to plan of work to meet regulatory market compliances as per QbD guidelines.
- Performing Literature search and conducting the pre-formulation studies under consultant&rsquos guidance.
- Planning and organizing day-to-day research activities & performing quality scientific experimentation as per Consultants design. Taking Consultants guidance to resolve any procedural problems as appropriate to the timely completion of research objectives.
- Properly documenting activities of the project under investigation under guidance of consultant. Preparation and Review of document like Product Development Report, Master Formula Card and Batch Manufacturing Record, product development report as per ICH, USFDA guidelines under consultant&rsquos guidance.
- Coordinating & continuous follow up with various departments like analytical development, purchase and store.
- Working under guidance of consultant for Execution of Scale up batches and Pre-Exhibit batches.
- Preparation and Review of document like CQA,QTPP, CPP and BOM.
- Initiating Change Control for scale-up batches.
- Supporting the activities of the R&D department, including safety performance, employee relations and quality.
Highest Qualification :-
M.Pharm / B.Pharm / M.Sc
Location :-
Akola
Minimum experience required in this position:
3+ years
Description:
Roles & Responsibilities :-
- Configuring and troubleshooting HPLC software and LIMS.
- Forming the data backup, data restore, archival & retrieval for all SCADA based equipment. Data Backup scheduling, and deploy system security policy 21 CFR part 11.
- Preparation & revision of all instrumentation, calibration & automation SOP&rsquos along with responsible to prepare IT SOPs and maintain documents as per SOP.
- Initiation of Deviations, CAPA, Change controls & preparing investigation reports Preparation of risk assessment and implementing mitigation plan.
- Preparation of Time synchronization planner, PLC preventive maintenance planner, data backup planner.
- Reviewing of PLC PM Check lists, time synchronization records, data backup records.
- Prime responsibility for CSV support and implementation at all over the plant (Production, Manufacturing, Laboratory department QC and other dept.).
- User role of administrator for all GxP applications, Like LIMS, Track and Trace System, SCADA, HMI, QC and other Laboratory Instrument.
- Troubleshooting technical problems and implementing solutions. Responsible for the fast and accurate troubleshooting of reported faults.
- Purchasing of IT Equipment and software in line within agreed budgets.
- Regular Monitoring of Production Application and Database. Configuring and installing the Printers. Providing technical support via helpdesk systems for a wide range of internal & external applications.
- Maintaining the Bio metric system. Maintaining the EPABX system. Calibration Spares maintenance. Maintaining up to date Antivirus on all machines company wide.
- Works with vendor support contacts to resolve technical problems with desktop computing equipment and software. Managing helpdesk, Mailbox, MS office, Active directory. Managing SCCM (System Centre Configuration Manager).
- Maintenance & management of the Critical Windows based Server Environment.
- Ensuring Active Directory Accounts, Configuration of laptops. To define user right matrix, User level role creation and set user privilege rights. Technical support for GxP application and compliance.
- Cyber roam security monitoring and implementation of different policy, monitoring of bandwidth utilization, VPN connectivity to access plant application, and security patches update.
- Implementation of (GLP & GxP Policy) Laboratory system control policy to ensure21 CFR part 11 Compliance.
- To perform software validation with Internal GLP Team and Respective service Engineer (IQ, OQ & PQ) of new or existing Lab software and PRM challenge test
Highest Qualification :-
Any Graduate in Computer / IT Field
Location :-
Akola
Minimum experience required in this position:
6+ years
Description:
Roles & Responsibilities :-
- Managing all the Analytical development activities of R&D Department
- Providing strategic leadership and technical expertise in analytical method development for release and stability testing of drug substance, raw materials, intermediates and drug product
- Identifying analytical science capabilities and technology tools needed to enable manufacturing process development, QC testing, and new drug candidate formulation development
- Applying scientifically‐driven thinking to the development of scientifically sound, well understood, and robust analytical methods
- Leading the trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary
- Leading analytical method transfer, qualification and validation to commercial QC and as needed for contract laboratories.
- Developing phase‐appropriate quality control strategy for drug substance and drug product
- Coordinating with other internal departments as and when required
- Managing product stability study programs of R&D batches
- Leading development of scientifically sound and data driven specifications
- Reviewing and providing technical reports, documents, batch analyses, analytical methods, reference standard, etc. for regulatory submissions
- Assist in the investigation and root cause analysis of analytical quality issues, including OOT/OOS results, generated during a study and execution of associated CAPA according to internal quality procedures
Highest Qualification :-
B.Pharm / B.Sc / M.Sc
Location :-
Akola
Minimum experience required in this position:
3+ years
Description:
Roles & Responsibilities :-
- Execute Analytical method Development activities of drug products based on QbD principles and regulatory requirements.
- Execution of Analytical Method validation activities for drug products as per the regulatory requirements.
- Execute routine Analytical Research activities of drug products.
- Establishing In-house systems and procedures to ensure cGLP practices & regulatory requirements for analytical activities at In-house R&D facility.
- Trouble shooting related to Testing methods, Stability studies, test results and designing of additional experimentations as necessary
- Execution & coordination for Analytical method transfer activities of drug products.
- Calibration of the Analytical instruments as per the master calibration schedule.
- Technical assessment & Analysis of drug substances (API) for projects execution.
- Review & clearance of technical documents leading to dossier batches executions and registrations.
- Preparation and review of Specifications, Method of analysis procedures and Analytical development reports.
- Preparation and review of analytical protocols and reports (Analytical method validation, Method feasibility, Analytical method transfer, etc.).
- Technical assessments of projects (Screening, pipeline and development projects stages) & Literature search).
- Preparation of analytical technical documents for dossier / Technology transfer executions / Regulatory submissions of projects.
- Assisting and resolving technical queries raised during Technology transfer activities & regulatory submissions.
- Assisting in establishment of In-house Infrastructure (Analytical equipment&rsquos Qualifications and preparation of SOP&rsquos).
- Assessment & coordination on regulatory deficiencies.
- Assisting with analytical requirements in finalization of project costings.
- Assisting in assessment of Analytical testing labs etc.
- Any other specific functional activities as given by Reporting Head.
Highest Qualification :-
B.Pharm / B.Sc / M.Sc
Location :-
Akola
Minimum experience required in this position:
2+ years
Description:
Roles & Responsibilities :-
- Independently develop and/or optimizes analytical methods.
- Developing and validating methods for testing of batches of drug substance and finished products (batch release testing and stability testing) according to ICH and Indian/WHO/EU/US requirements.
- Developing and validating test methods used in cleaning validation.
- Coordinate analytical transfer to QC laboratories.
- Preparing analytical method development reports, as well as ICH/EU compliant analytical validation protocols and reports.
- Preparing specifications.
- Writing/reviewing of SOPs.
- Participate in annual review of suitability of analytical methods and contribute to Annual Product Quality Reports (PQRs).
- Supporting on all analytical activities.
- Participating in self inspections and regulatory inspections (Indian, WHO, EU).
- Completing any other designated tasks, as necessary.
Highest Qualification :-
B.Pharm / B.Sc / M.Sc
Location :-
Akola
Minimum experience required in this position:
2 years
Description:
Roles & Responsibilities :-
- Microbiologists undertake laboratory analysis and monitoring of microbial cultures, samples and new drugs
- Planning and carrying out trials tracking environmental microorganism development growing microbe cultures.
- Developing new pharmaceutical products, vaccines, medicines and compounds such as antiseptics.
- Collecting samples from a variety of locations.
- Recording, analyzing and interpreting data.
- Writing research papers, reports and reviews, keeping up to date with scientific and research developments ensuring that data is recorded accurately in accordance to guidelines.
- Observing high health and safety standards and managing laboratories
Highest Qualification :-
D.Pharm / B.Pharm / M.Pharm
Location :-
Akola
Minimum experience required in this position:
6+ years
Description:
Roles & Responsibilities :-
-
Manage the setting up of the new Plant's QC & Microbiology lab along with and system development, implementation.
-
Manage the development, Review and Approval/troubleshooting of protocols and reports such as method validation, method transfer, process validation, stability etc.
-
Manage, plan and direct the work activities of QC & Micro labs to ensure lab testing provide the highest quality analytical support for manufacturing in a timely and compliant manner while ensuring compliance with protocols, cGLP and safety regulations.
-
Provide leadership, management, evaluation and training to all laboratory employees.
-
Execute and approve all laboratory working along with Review and investigation of all laboratory data outside of trend.
-
Ensure all vendors have been qualified and adhere to vendor qualification standards with the aim of optimal utilization of the reduced testing procedure.
-
Establish and implement a KPI structure to ensure optimal test/cost ratio.
-
Working in coordination with other departments to ensure Plant's compliance to QMS.
Highest Qualification :-
D.Pharm/ B.Pharm/ M.Pharm
Location :-
Akola
Minimum experience required in this position:
2+ years
Description:
Roles & Responsibilities :-
- Doing management of lab chemicals, reference standards, impurities, etc.
- Making calibration of laboratory instrument
- Doing sampling and analysis of water, RM & PM.
- Preparing Reagent and Volumetric Solutions
- Calibrating and handling of Karl Fisher, Autotitrator, Dissolution, UV-Visible, FTIR, Viscometer and Polarimeter
- Preparing specification and STP
- Doing analysis of In-Process and finish product
- Following instructions given by HOD
Highest Qualification :-
B.Sc / M.Sc (Chemistry/ Microbiology)
Location :-
Akola
Minimum experience required in this position:
3+ years
Description:
Roles & Responsibilities :-
- Installing and Maintaining, trouble shooting of all Process equipment of OSD.
- Maintaining Installation, Validation, calibration of type of equipment&rsquos used in Company
- Ensuring estimation and implementation, effective utilization of resources
- Writing reports and GDP documentation Analyzing and interpreting data
- Collaborating with a team of engineers from Production/Quality / Supplier & Engineering to provide required assistance.
- Ensuring smooth functioning of Tablet Mfg. & packing equipment's
- Having knowledge on SAP, Track wise, GDP, GEP etc.
- Maintaining awareness of PLC/SCADA trouble shooting, qualification/validation as per requirements.
- Having good knowledge of DCS, PLC, HMI and SCADA specification, control system architecture.
- Having good knowledge of panel wiring drawings, hardware and software FAT protocol, IQ, OQ.
Highest Qualification :-
B.E./M.E.
Location :-
Akola
Minimum experience required in this position:
5+ years
Description:
Roles & Responsibilities :-
- Supporting in investigation of Incident, OOS and OOT to identify the root cause.
- Reviewing of specification, MOA of In-process and Finished products.
- Ensuring validity of all testing data, raw data, Audit trail of QC instruments and ensuring its adequacy, accuracy on periodic basis.
- Reviewing of analytical reports of RM, PM, In process, Finished Goods.
- Reviewing analytical method validation protocols, Report, analytical method development report for routine analysis against the actual raw data, transfer, and stability protocol & summary report.
- Monitoring daily GLP practices in the QC areas & ensuring adherence.
- Ensuring compliance of training, validation and quality function pertaining to adherence with documents, system and procedure in accordance with the current regulatory expectation
- Ensuring compliance for document issuance, distribution, retrieval and archival as per the procedure.
- Reviewing and ensuring compliance of retention sample and stability reports as per the procedure.
- Maintaining QC Laboratory&rsquos Quality System.
Highest Qualification :-
M.Sc / B.Pharm
Location :-
Akola
Minimum experience required in this position:
2+ years
Description:
Roles & Responsibilities :-
-
Responsible for receipt and storage of all raw /packing materials in the formulation warehouse.
-
Preparation of GRN and maintaining the stock ledger.
-
Responsible for dispensing of raw/packing materials as per the production plan.
-
Responsible for proper palletisation and loading of the finished goods for dispatches.
-
Responsible to follow the systems, procedures and practices for smooth warehousing operations.
-
Responsible for handling of materials and retest and rejected materials.
-
Making online entries in the log books and other records maintained in the warehouse.
-
Ensuring the timely maintenance of all equipments and trucks and trolley ensuring it is in working condition at all times.
-
Ensuring shifting and storage of correct material in the location after sampling and approval/rejection of materials.
Highest Qualification :-
Any Graduate
Location :-
Akola