Store Manager

Quality Assurance Associate

Associate I, Quality Operations

Sr P&PM Analyst (Treasury Planning)

Lead Planning & Performance Management Analyst - SCD

QC Chemist I

Senior Business Analyst

Senior Transport Analyst

Refining/NGL Field Metals Mechanic

Supply Planning Manager

Responsibilities: <ul><li>You’ll be in the driver’s seat as the leader of amazing team members.&nbsp;</li><li>At the company, our managers use their valuable skillz and run their very own store.&nbsp;</li><li>In this role, you’ll oversee the operational plan of your store and team.&nbsp;</li><li>You’ll also create a customer-focused environment while developing &amp; maintaining a fully-staffed store - all while maximizing your store’s profitability.</li></ul> Requirements: <ul><li>3 years’ experience supervising others.</li><li>High school diploma or equivalent.</li><li>Strong leadership, managerial and communication skills.</li><li>Understanding and commitment to our client mission, vision and TCF (Total Customer Focus).</li></ul>

Responsibilities: <ul><li>Primary responsibilities of this role include the following:</li><li>With Supervision, review documents/records and provide batch release authorization to 3PL service provider for products manufactured outside of the US.</li><li>Support Drug Product Complaint management; forwarding to respective drug product manufacturing site and coordinate with corporate QA for investigations.</li><li>Support Drug Product Recall/Field alert management.</li><li>Assist with review of Quality Agreements.</li><li>For applicable products, coordinate with Contract Testing Laboratories for Analytical Method Transfer activities, Drug Product testing, any OOS results, and test method issues.</li><li>With supervision, review deviations/investigations related to the companys frontend products.</li><li>Assist with SOP management for the company’s US corporate office.</li><li>Support with quality matters for disposition of product returns.</li><li>Assist during FDA inspections and local regulatory inspections at the company’s US corporate office.</li></ul> Requirements: <ul><li>Excellent verbal and written communication skills are necessary.</li><li>With supervision and direction, effectively prioritizes competing tasks in a fast-paced and dynamic environment.</li><li>Motivated, results driven with attention to detail, accuracy and clarity.</li></ul> Qualifications:&nbsp; <ul><li>BS degree in Pharmacy, Chemistry, Biology or Microbiology is preferred. 1-2 years of Quality Assurance or related pharmaceutical industry experience is preferred.</li><li>Recent graduates will be considered for this role.&nbsp;</li></ul>

Responsibilities: <ul><li>The Quality Associate I, Operations is responsible for actively participating in “on the floor” Quality activities during product manufacturing and/or packaging.</li><li>Quality activities include product sampling and inspection, area clearance to confirm process readiness, and non-conforming event support to resolve in-process issues.</li><li>Communicates to multiple departments and supervision to provide timely process and issue updates.</li><li>Identifies and escalates issues or problems to appropriate supervision. Participates as a team member on cross-functional teams.</li><li>Participates in reviews and structured processes for continuous improvement.&nbsp;&nbsp;</li></ul> Quality Operations: <ul><li>Performs physical inspection of in-process and finished product samples as assigned and according to the production schedule.</li><li>Collects samples from manufacturing and packaging according to the defined Batch Production Record and procedure requirements.</li><li>Becomes competent in processes: Weighing, Blending, Granulation, Compression, Coating, Encapsulation, Packaging.</li><li>Follows internal processes related to controlled substances.</li><li>Performs GMP related verifications such as line clearances, cleaning, room inspection, and materials</li><li>Collects and appropriately labels packaging retain samples, and submits to the archive storage</li><li>May execute computer data entries in CME, JDE, LIMS, and/or department databases.</li><li>Collects retain samples and performs sample evaluation for Annual Product Review.</li><li>May backup third party product review/release.</li><li>Perform sampling of Active Pharmaceutical Ingredients, excipients, and packaging components for release testing.</li></ul> Non-conforming events: <ul><li>Responds to and escalates events identified during production to Quality Management.</li><li>Participates in investigations with the Rapid Response Team as needed.</li></ul> Process Improvement: <ul><li>Collaborates with Manufacturing and Quality partners to identify and implement improvements.</li></ul> Compliance: <ul><li>Conducts GMP walkthroughs of facilities</li></ul> <ul><li>Learns how to perform in-process audits to identify adherence to SOPs and BR requirements.</li><li>Actively participates in training events, and maintains currency with assigned training requirements.</li></ul> Safety: <ul><li>Follows all procedures to ensure a safe and compliant work environment.</li></ul> Requirements: Education &amp; Experience: <ul><li>High school diploma or equivalent with 2-4 years of relevant industry experience (Oral Solid Dose pharmaceutical manufacturing and Quality Assurance experience preferred)</li><li>Ability to communicate and work with teams.</li><li>Attention to detail.</li><li>Strong documentation skills.</li><li>Ability to read and interpret SOPs and function within the scope of procedures.</li></ul>

Responsibilities: <ul><li>Lead, coordinate and execute, with minimal supervision, routine planning and performance management tasks, such as the weekly highlights, monthly reporting, quarterly business reviews, accountability reporting, KPI reporting, and business plan development;</li><li>Assume the risk coordinator role for the Admin Area;</li><li>Represent the Admin Area on cross-functional initiatives relating to planning and performance management;</li><li>Develop and maintain a working knowledge of the major deliverables of the Admin Area through hands-on involvement in these activities;</li><li>Provide oversight on the Admin Area’s administrative costs</li></ul> Requirements: <ul><li>Bachelors in Business Admin, Finance, MIS or a related discipline</li><li>5-7 years of related experience</li><li>Ability to produce reports and presentations to senior management;</li><li>Ability to work effectively within a multi-cultural and multidisciplinary team, as well as in cross functional settings;</li><li>Excellent communication skills; proficient in developing spreadsheets in Excel and presentations in PowerPoint;</li><li>Enthusiasm to develop knowledge and skills relating to the Treasury functions;</li><li>Attention to detail is a must.</li></ul>

Responsibilities : <ul><li>Provide analytical findings and recommendations relating to regular P&amp;PM tasks, such as business plan preparation, performance tracking measurement, and performance analysis and accountability reporting.</li><li>Conduct special P&amp;PM-related studies, such as the development of performance initiatives and business cases, benchmarking, risk management, design and redesign of measurements, processes and workflows, and information system-related changes.</li><li>Provide supervision, coordination and/or facilitation in the execution of regular and special tasks by other P&amp;PM personnel, as well as mentorship on P&amp;PM analytical practice.</li><li>Perform other related staff and analytical duties, as assigned.</li></ul> Requirements : <ul><li>As the successful candidate, you will hold a Bachelor’s degree in Business, Engineering, or a related discipline.&nbsp;Possession of an advanced business degree (e.g., MBA) and/or relevant professional certification (e.g., CMA, CFA, CPA) is preferred.</li><li>You should have 12 years of related experience, including a demonstrated capability and track record, in the practice of planning and performance management, and in the use of business intelligence tools.</li><li>Possess solid knowledge and understanding of management accounting, finance and Excel.</li><li>Previous experience in Oil &amp; Gas is preferred but not required</li><li>Have an excellent command of oral and written English</li></ul>

Responsibilities: <ul><li>The Chemist I, under direct supervision, learns and performs QC laboratory chemical analyses of raw materials, in-process materials, stability and finished products, and testing to support process validation.</li><li>May participate in investigations.</li><li>Learns and stays current with regulatory guidances and compendia relevant to laboratories and pharmaceutical manufacturing.</li><li>Conducts routine laboratory analyses: finished product testing, stability testing, raw material testing, cleaning verification testing and manufacturing in-process testing.</li><li>Typical activities may include buffer/solution preparation, standard preparation and operating analytical instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.&nbsp;</li><li>Uses laboratory software for analyses.</li><li>Provides general laboratory support such as routine instrument cleaning/preventative maintenance/calibration, sample receiving, chemical inventory, document filing and housekeeping</li><li>Cleans lab working surfaces and disposes of any excess chemicals, solutions, solvents, etc. in the special waste containers for each class of waste chemicals.</li><li>Under close supervision, learns to troubleshoot basic instrument problems.</li><li>With guidance, participates in OOS/OOT/NOE and other investigations.</li><li>Elevates questionable sample results, OOS, and aberrant results immediately to Supervisor.</li><li>May assist in drafting, editing, and reviewing SOPs and laboratory investigations.</li><li>Maintains assigned training records current and in-compliance.</li><li>May assist in the training of less senior laboratory staff.</li><li>Performs assigned work in a timely and safe manner conforming to regulatory, company and compendiaI requirements within pharmaceutical manufacturing setting.</li><li>Document accurately data generated in notebooks/worksheets/LIMS in compliance with SOPs.</li><li>Follows internal processes related to controlled substances continuous.</li><li>Follows EH&amp;S procedures to ensure a safe work environment.</li><li>Follows all applicable safety and standards guidelines, such as SOPs, cGMP, DEA regulations good documentation practice and/or MSDS continuous.</li></ul> Requirements: <ul><li>Minimal acceptable level of education, work experience and certifications required for the job.</li><li>Bachelor of Science Degree in chemistry, chemical engineering or related field with analytical chemistry coursework required.&nbsp;</li><li>Some pharmaceutical laboratory experience preferred.</li><li>Proficiency in a body of information required for the job.</li><li>e.g. knowledge of FDA regulations, GMP/GLP/GCP, Lean Manufacturing, Six-Sigma, etc.</li><li>Proficiency with various laboratory techniques/instruments: HPLC, UV-Vis, FT-IR, GC and dissolution tester, melting point apparatus, viscometer, Karl Fischer titrator, pH meter, analytical balance, etc.&nbsp;</li><li>Basic knowledge of wet chemistry techniques.</li><li>Knowledge of applicable safety and standards guidelines: SOP, cGMP, GLP, DEA regulations and/or MSDS.</li><li>Competency in Microsoft Office Suite.</li><li>Often referred to as “competencies”, leadership attributes, skills, abilities or behaviors that may be enterprise, functional or job specific e.g. coaching, negotiation, calibration, technical writing etc.</li><li>Ability to display and analyze data in a logical manner.</li><li>Good verbal and written communication skills as well as good computer skills.</li><li>Attention to details and accurate record keeping.</li><li>Establish and maintain cooperative working relationships with others</li><li>Solid organizational skills.</li><li>Ability to take initiative, set priorities and follow through on assignments.</li><li>Physical &amp; mental requirements e.g., lift 40 pounds, walk across plant/warehouse, business travel (% of time), driving as part of work responsibilities, etc.</li><li>Extended periods of sitting, standing, walking, reaching, climbing/balancing, kneeling/crouching/crawling, looking at monitor for extended periods, moderate noise levels and potential business travel. Work is in an FDA and DEA-regulated pharma lab environment with risk of exposure to various chemicals</li><li>Must occasionally lift and/or move up to 15-25 lbs.</li><li>Ability to wear personal protective equipment, including respirators, gloves, etc.&nbsp;</li><li>Specific visions abilities are required by this job include close vision and color vision.</li><li>Ability to occasionally tolerate significant differences in temperature and/or humidity for short periods.</li></ul>

Responsibilities: <ul><li>Works with little or no supervision on projects of moderate to high complexity and independently on projects of low to moderate complexity.</li><li>Serves as liaison between our Business Development, Development and Quality Assurance teams.</li><li>Serves as the primary technical contact with carrier partners and certification teams.</li><li>Contributes to the identification of solutions, elicitation and development of business and functional requirements that meet the needs of the business in a date driven business and application development environment.</li></ul> Requirements: <ul><li>Minimum 7 + years in Business Requirement Gathering/Product Design</li><li>Experience in Business Requirement Gathering/Product Design</li><li>Worked extensively in conversion of Business to Technical Specifications</li><li>Showcased Strong Analytics experience&nbsp;</li><li>Hands on experience in handling transition projects</li><li>Use-cases, IIBA (or similar), Enterprise Architect</li><li>IIBA CBAP (Certified Business Analysis Professional)</li><li>Logistics Domain Knowledge</li><li>International Trade Knowledge</li><li>Having Product Owner Experience is add on benefit</li><li>Highly experienced in Requirements elicitation and documentation analysis</li><li>Hands-on experience with Software Development tools and ability to perform some scripting tasks</li><li>Knowledge of Microsoft Office and other documentation tools</li><li>Bachelors Degree (or internationally comparable degree) in Computer Science or related field - Preferred</li><li>Experience with Carrier business rules and industry standards – Preferred</li></ul>

Responsibilities: <ul><li>Analyzing policy changes in transportation: Identifying trends in policy including environmental standards affecting different modes of transportation.</li><li>Modelling vehicles forecast: development of pragmatic car sales forecasts by country informed by current fleet, fuel consumption regulations, along with other variables.</li><li>Develop dashboards and report on mobility modes: provide insights on changes for different modalities in different regions.</li><li>Managing multiple projects: Prioritizing tasks and projects to meet deadlines and organizational goals.&nbsp;</li><li>Represents company at industry conferences and seminars.</li><li>Travel is required one or two times a year.&nbsp;</li><li>Fosters and supports company culture and values.</li><li>Team and goal oriented. Builds trust.&nbsp;</li></ul> Requirements: <ul><li>Degree: Bachelor’s or master’s degree in planning, engineering (transportation, vehicle, electrical), economics, or related field.&nbsp;</li><li>Work experience: Five years (or more) experience in private sector, academia or government research with a focus on transportation, energy, environment, and policy.&nbsp;</li><li>Languages: Fluency in English (oral and written) is must.&nbsp;</li><li>Effective written and oral communication skills along with superior quantitative skills to analyze large datasets, drafting papers and publications.&nbsp;</li><li>Ability to work effectively with minimum supervision and on relatively unstructured tasks.</li><li>Must be able to work on time-sensitive environment and reacts quickly with requests.&nbsp;</li></ul>

Responsibilities: As the successful candidate you will be required to perform the following: <ul><li>Install, maintain and repair piping systems in an industrial facility, including pipework, pressure vessels, heat exchangers, boilers and ancillary equipment.</li><li>Determine the nature of repairs to be made and replacement parts required.</li><li>Perform cut, thread, bend, join, remove, install and assemble carbon steel, stainless steel and non-metallic pipe fittings.</li><li>Remove, repair and install tubes in heat exchangers and condensers.</li><li>Clean, and repair boiler tubes and burners as well as install, expand and plug boiler tubes.</li><li>Perform minor rigging operations and assist rigging crew on large lifting operation.</li><li>Perform piping hydro-test.</li></ul> Requirements: <ul><li>You must hold an associate degree in mechanical and fabrication engineering from a recognized and approved program an advanced degree is preferred.</li><li>You must have a minimum of eight years’ experience with providing work direction, technical guidance, and supervision for work crews in the fabrication, welding, and repair of plant pressure vessels, piping, and auxiliary equipment.</li><li>You must have a full understanding and adherence of all work permit type requirements.</li><li>You must have a full understanding of all field mechanic and fabrication principles.</li><li>You should be able to demonstrate strong analytical and troubleshooting skills in the field of piping and construction installation.&nbsp;</li></ul>

Duties and Responsibilities Location : Bengaluru, IndiaJob Purpose and ImpactThe Supply and Inventory Planner II will contribute to coordinating long term supply chain strategies across networks to address capacity issues and production location decisions in support of business goals. In this role, you will monitor key integrated business planning performance indicators, cost to serve performance data and help coordinate cross functional work teams to meet high customer service standards.&nbsp;Key Accountabilities<ul><li>Maintain data relevant to network distribution planning activities including capacity, constraint, logistics, supplier, master and location data.</li><li>Generate and execute cycle and safety stock plans for the assigned product or location, using the approved supply plan inputs.</li><li>Develop gap coverage plans during inventory shortages.</li><li>Create requirements plan and long term supply plan for assigned products and locations as input for the integrated business planning cycle.</li><li>Independently solve moderately complex issues with minimal supervision, while escalating more complex issues to appropriate staff.</li><li>Other duties as assigned</li></ul> Requirements <ul><li>Qualifications</li><li>Minimum Qualifications</li><li>Bachelors degree in a related field or equivalent experience</li><li>Minimum of two years of related work experience</li><li>Other minimum qualifications may apply</li><li>Preferred Qualifications</li><li>Three years of experience with at least one in supply and inventory planning</li></ul>

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47 supervision Jobs found

Store Manager

Quality Assurance Associate

Associate I, Quality Operations

Sr P&PM Analyst (Treasury Planning)

Lead Planning & Performance Management Analyst - SCD

QC Chemist I

Senior Business Analyst

Senior Transport Analyst

Refining/NGL Field Metals Mechanic

Supply Planning Manager

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47 supervision Jobs found

Store Manager

Quality Assurance Associate

Associate I, Quality Operations

Sr P&PM Analyst (Treasury Planning)

Lead Planning & Performance Management Analyst - SCD

QC Chemist I

Senior Business Analyst

Senior Transport Analyst

Refining/NGL Field Metals Mechanic

Supply Planning Manager

WhiteCrow WhiteCrow is on a mission to connect companies with the best talent across the globe.

EMPLOYER

TALENT

COMPANY

Contact Us

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WhiteCrow
WhiteCrow is on a mission to connect companies with the best talent across the globe.