Lancesoft Indore Jobs in Usa

Title: Biotechnologist Associate Location: Portsmouth, NH – 03801 Duration: 12 Months Nights
- 7 PM
- 7 AM
- rotating days
- every other weekend.

Description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions.

Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment.

They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.

• Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.

• Attain qualification for all assigned tasks and maintain individual training plan.

• Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.

• Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.

• Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.

Must be willing to gown and work in a "clean room" environment.

Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.

• Perform other duties as assigned.

Job Title: Pharmaceutical Formulation Technician/Manufacturing Pharmaceutical Technician- Duration: 06 Months Location: Wilson NC 27893 Granulation/Blend/Bead Coating) Onsite – 2nd shift (4pm- 2:30am, Mon-Thurs) Job Summary · The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.

Primary Responsibilities Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.

Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.

Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures.

Operates scales including set-up, verification, leveling and challenging.

Identify, report, and resolve quality issues.

Safely and in compliance with batch records and SOPs, set up, operate, and clean manufacturing equipment (oral solid dose manufacturing may include rotor sieves, granulators, blenders, coaters, encapsulators, compression machines, etc.).

Perform in-process testing and inspections as required by Master Batch Record (weighing, tablet thickness, tablet hardness, friability, visual inspection, etc.).

Clean and sanitize manufacturing rooms including walls, floors, and ceilings per SOPs.

Report accidents and unsafe conditions or unusual circumstances to supervisor.

Complete accurate and timely documentation.

Follow good documentation practices in accordance with GMP.

Actively participate in Production team and Site communication meetings.

Maintain regular and punctual attendance; work overtime as required.

Support GMP investigations and events.

Identify and report potential GMP impacting situations.

Contribute to Standard Operating Procedure (SOP) writing in your technical area.

Education and Experience Requirements High School Diploma or equivalent.

Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.

Necessary Knowledge, Skills, and Abilities General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division.

Understanding of the Metric System of Measurement.

Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.

Title: Pharmacist Location: Fort Worth, TX USA 76177 Duration: 02/09/2026 to 05/09/2026 Work schedule: M-F 9-6 temp Onsite Role 1.

must be licensed in both NC and CA 2.

license must be in good standing 3.

must enjoy being on the phone for 8 hours a day Job Description: Professional Meets or exceeds current CE requirements pursuant to Board of Pharmacy Laws Supports professional development goals of staff within the assigned patient care team Maintains an attitude of constant learning and ensures self-education within the pharmacy arena Attends conferences with Peers and reports topics discussed at staff meetings Qualifications/Requirements 3-5 years or more post-graduate experience in pharmacy operation, clinical oversight, and patient care Graduate of an accredited school of pharmacy BCOP certified or willing to become BCOP certified when eligible Current and unrestricted license in good standing Licensed in the state of North Carolina, Texas, or Kentucky to practice pharmacy, license in good standing Meets or exceeds current CE requirements pursuant to Board of Pharmacy Laws Ability to apply for additional state licensures as needed Excellent oral and written communication skills Working knowledge of computers and excellent word processing skills Working knowledge of sterile technique and other quality control issues Responsibilities Conducts a comprehensive clinical review of pharmacotherapy for each patient including drug utilization, counseling, compliance, drug interaction screening, side effect profiling and drug administration support to ensure the patient’s treatment plan is in line with evidence-based recommendations Documents result of pharmacotherapy review in patient chart so that the nursing team performing follow-up assessments are aware and educated Counsels patients on new drug therapy in accordance with clinical management models so that patients are educated on the specifics of their planned treatment Completes REMS training and follows program SOPs accordingly Coordinates patient care with the referring clinician, including but not limited to, social, psychological and physical needs that warrant customized services by Biologics, Inc.

(i.e.

pre-filled syringes, color coded labeling for medication identification, etc.) and documenting these services in their progress note so that the fulfillment and distribution teams are aware of additional materials to add Serves as a Liaison between patients, caregivers, home health agency nurses, hospice nurses, and the prescribing physician/clinician for orders related to the services provided by Biologics, Inc.

to ensure all stakeholders receive outrageous customer service Provides subcutaneous teaching support for patients and caregivers.

If necessary, coordinates adequate nursing services with the prescribing clinician Provides on-call coverage at direction of Pharmacist-in-Charge so that patient’s needs are met outside of operational hours Processes prescriptions accurately and timely so that subsequent groups Verifies the discontinuation of service for each patient by assigning the appropriate therapy outcome and deactivates the patient’s chart, prescriptions and software profile as appropriate so that the Patient Support group is informed to discontinue future refills.

Implements clinical management models for products and disease states Primary intake for all new team referrals initiated by telephone Committed to “outrageous customer service” as defined by Biologics’ internal policies Understands the importance of relationship building with patients and clinicians and works to foster such relationships Operations Strict adherence to company policy as it relates to all government funded payers, specifically Medicaid and Medicare Dispenses all medication pursuant to a physician’s order and in accordance with all state, federal and board of pharmacy laws Compliant with all company policies specifically as they relate to pharmacy operations Adheres to the federal and state laws with regard to the purchase and dispensing of controlled substances Verifies accuracy of prescription order entry so that errors or discrepancies are corrected early in the workflow, making the process more efficient for other groups Verifies accuracy and quality assurance check of final prescription product dispensed Assists pharmacy technicians in adjudication of pharmacy claims to ensure accurate payment is communicated and collected Monitors hazardous waste material management within the pharmacy Understands and supervises the aseptic technique of pharmacy personnel Oversees pharmacy technicians Utilizes patient education materials effectively Perform intake of and ensure appropriate reporting of adverse events and product quality complaints as applicable and in accordance with regulatory and contractual obligations.

Contract Duration: 06 Months Job Summary · The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines.

Primary Responsibilities Follow Master Batch Records for the manufacturing of controlled, oral solid dose (OSD) and other dosage forms when required.

Prepare raw materials, blends, and bulk accountability throughout manufacturing processes.

Performs weight checks for incoming and dispensed materials ensuring compliance with established procedures.

Operates scales including set-up, verification, leveling and challenging.

Identify, report, and resolve quality issues.

Education and Experience Requirements High School Diploma or equivalent.

Up to three years pharmaceutical industry experience preferred or an equivalent combination of education, demonstrated mechanical skill, and experience in a similar industry.

Necessary Knowledge, Skills, and Abilities General ability to perform basic to complex mathematical computations of addition, subtraction, multiplication, and division.

Understanding of the Metric System of Measurement.

Preferred experience in oral solid dose (OSD) pharmaceutical manufacturing Granulation/Blending and Bead Coating operations.

Description: The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing production suites.

They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by client’s contracted cleaning staff.

They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique and cross contamination awareness in handling of products and materials.

Key Responsibilities: Perform 6S and stock each suite daily, clean soiled parts daily.

Determine production needs for autoclaved assembles and deliver to suites.

Perform daily and weekly maintenance activities on analytical equipment.

Perform weekly and monthly cleans of inoculum rooms.

Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.

Attain qualification for all assigned tasks and maintain individual training plan

Job description: To ensure that the QC testing of all products is performed to GMP and company standards.

This involves analytical/microbiological testing (as applicable), analyzing samples, recording, evaluating and reporting data using prescribed procedures with limited or no supervision Conduct routine analytical testing of raw materials, packaging materials, finished products and environmental samples using approved methods and various instrumentation, Generate valid data at expected levels of productivity while adhering to cGMP.

Maintain and troubleshoot laboratory instruments.

Assist in training other laboratory personnel on methods, instrumentation and computer systems.

Participate in interdepartmental project teams or committees.

Understand data integration and calculation of results Education: BS.

in Microbiology, Biology

Job Description: This is a laboratory-based position within the Vaccines Early BioProcess Analytical Development group.

The individual will perform routine sample testing, analytical method development and assay qualification studies in support of early vaccine development.

Assays include but are not limited to enzyme-linked immunosorbent assays (ELISAs) and other plate-based testing.

This is a dynamic position that will require work on fast-moving and high-visibility projects.

Basic Qualifications: BS or BA degree in biology or related discipline with 2 years relevant experience.

Basic knowledge of antibody-antigen interactions and bioassay analytical techniques.

Strong verbal and written communication skills.

Proficiency with personal computers including word processing, spreadsheets, PowerPoint and relevant scientific software is required.

Preferred Qualifications: Prior experience working with plate-based immune methods.

Previous experience with automation (ie.

Hamilton STAR).

Experience with documentation using electronic laboratory notebooks.

Contract Duration: 08+ Months Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: High School diploma Must have basic math skills Must have reading and writing comprehension of the English language Flexibility to work extended hours to achieve results.

Ability to lift up to 50 lbs nicator using both oral and written skills used at all levels of the organization Preferred Qualifications: If you have the following characteristics, it would be a plus: 1 year of recent or consistent experience in a high energy, fast paced, cGMP warehouse or manufacturing environment.

SAP or WMS system experience Self-starter/ Self motivated Ability to work with little supervision.

Effective commu

Contract Duration: 06 months Duties: Performing beginning calibration activities.

Basic mechanical, pressure equipment verification to support internal customers.

Potential to run some automated system calibrations.

Working in the calibration lab, some data entry duties Experience: 1-2 years’ of experience; Testing of equipment, Lab experience is plus, Test Tech of equipment, analysis work, scientific notation, unit conversions (measurements) Education: HS diploma or equivalent work experience in a related field (Master degree may be over qualified) Associate degree will be considered with experience.

Key Skills: Computer experience with excel.

Read and follow written instructions.

Inquisitive and eager to learn.

Attention to detail.

Ability to work as a team member.

Key Responsibilities: Responsible for direct raw and pack materials for a subset of SKUs.

Run material forecasts weekly based on new weekly production schedule to assist the materials management team.

Responsible for covering production while keeping material inventory low to minimize any material waste down the road.

Work with HQMM team and cross functional team members on commercialization project trackers to ensure timeline is met while mitigating material waste.

Attend Commercialization Meetings to cover Supply Planning follow ups and actions, and other supply cross functional meetings as needed.

Qualifications: Bachelor's degree in Supply Chain Management, Business, Operations, or a related field.

2+ years of experience in materials management, supply planning, inventory management, or a similar role, preferably within a large CPG environment Strong analytical, problem-solving, and decision-making skills.

Proficiency, or ability to learn quickly, in ERP systems (e.g., SAP, Oracle) and advanced planning tools.

Excellent communication and collaboration skills.

PowerBI / Tableau exposure preferred.

Advanced Excel

Position Summary: The Packaging Operator is responsible for operating packaging line equipment, handling materials, and ensuring compliance with safety, quality, and regulatory standards.

This role requires attention to detail, adherence to SOPs, and effective communication to maintain smooth and efficient packaging operations.

Education Required High School Diploma or Equivalent Required Experience Required: 1-2 years’ experience in FDA regulated packaging environment desired.

Specialized or Technical Knowledge, Licenses, Certifications required Proficient in navigating HMI screens for various packaging equipment, including Tablet/Capsule Filler, Cottoner, Capper, Desiccant Inserter, Checkweigher, Labeler, Case Former, and Pallet Jack.

Ability to assist Packaging Technicians during line changeovers.

Capable of working extended hours and maintaining focus under challenging conditions.

Description: This engineer works within or on the test and reliability team and/or a project team, generally within the molecular R&D project group.

This engineer will use experience and education to test and evaluate electromechanical medical devices to identify product limits and to identify and evaluate improvements throughout the products lifecycle.

This engineer uses experience and education to perform the types of engineering activities which are generally considered within the realm of test and reliability engineering and any other expertise that might be held by this particular individual.

This engineer is expected to work and communicate well with other team members and leadership as assigned in order to meet the goals of the project, the department, and the company.

Responsible for development of testing for electromechanical medical device throughout its product life cycle, including: Environmental testing (Temperature, Humidity, Altitude) Shock and vibration testing Reliability testing Ship testing Dust ingress Water ingress Electrical/EMC/EMI Develop Test Fixture Designs.

Develop and maintain test protocols and test plans throughout the development cycle (utilizing Helix ALM) for electrical and mechanical sub level testing and electromechanical system level testing.

Design Verification Testing Design Validation Testing Performs other duties as assigned.

Qualifications: B.S.

in Engineering or Equivalent.

10+ years of experience in an engineering field, testing field preferred.

Responsible for performing the activities associated with the preparation of vaccine components in an aseptic clean room environment utilizing virus and cell culture techniques according to USDA regulations Ensure compliance to the Standard Operating Procedures during execution of processes.

Assist with training and coaching of current and new employees on required skills Complete/Review in process documentation for accuracy and compliance in a timely manner; maintenance of technical data and support documentation Participate in root cause analysis and implement corrective and preventative actions to address problems; escalation of production flow disturbances Skills: Demonstrated strong organizational and time management skills with exceptional attention to detail.

Clean room and aseptic technique knowledge.

Basic understanding of Lean Manufacturing Principles Basic math skills, equipment/automation trouble shooting skills.

Proficient with Microsoft Office and other database software systems.

Excellent oral and written communication skills.

Ability to work in a team environment.

Demonstrated ability to problem solve.

Education: High School Diploma or equivalent.

Preferred Biology Degree or related field,one year or more of laboratory experience and/or manufacturing experience.